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Completed

NCT Number: NCT03886805

The Dual-task Training Under Different Priority Instructions on Gait Speed in Community-dwelling Older Adults

This study analyzed the effect of different modalities of dual-task training in the improvement of gait biomechanics, postural balance, falls episodes, executive functioning, and quality of life in community-dwelling older adults. Half of the participants have undertaken a dual-task protocol training with progression from variable-priority to fixed-priority instructions, while the other half have undertaken a dual-task protocol training under variable-priority instructions.

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Key information

Conditions

Gait Postural Balance

Age range

60 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Francis Trombini de Souza

Petrolina, Pernambucano, 56302685, Brazil

About this study

Although dual-task training for improving postural balance is an emerging interest area, the effects of dual tasks and dual-task training on static and dynamic postural stability remain unclear. Even though variable (alternating) instructional priority dual-task training has been shown higher effect than fixed (concurrent) priority dual-task training approach to improving the balance impairments, we must consider in everyday pragmatic situations, motor, and cognitive tasks are often demanded simultaneously and this requires an individual's attention toward an external source of attention while performing a primary task. Then, our rationale for this study is older adults who underwent a training protocol composed of a dual task with variable and fixed instructional priority will achieve better improvements regarding the studied variables in comparison to the group who will be submitted a protocol composed only by dual-task with variable priority training. Therefore, this protocol for a six-month, double-blind, randomized controlled trial with six-month follow-up post-training analyzed whether examine whether a dual-task protocol training with progression from variable priority to fixed priority instructions is effective in improvement of gait biomechanics, postural balance, falls episodes, executive functioning and quality of life in community-dwelling older adults.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Participants of both sexes
  • Age between 60 and 80 years old
  • Participants with a score greater or equal to 52 (up to a maximum of 56) in the Berg Balance Scale
  • Participants with a score greater or equal to 24 (up to a maximum of 30) in the Mini-mental State Exam
  • Participants who are able to walk uninterruptedly for a distance of 10-meter at a self-selected velocity of at least 1.0 m/s without the need from another person, cane or walker

Exclusion criteria

  • Self-report of two or more falls in the last 12 months
  • Any contraindication to balance postural training
  • Any contraindication to cognitive exercise training
  • With self-report of two or more falls in the last 12 months
  • Who is participating or have participated, in the last 6 months, in any regular and structured physical exercise program, for 3 or more times per week
  • Any chronic health condition, including cardiovascular disease, respiratory disease, stroke, active cancer, neurological or neuromuscular conditions whose exercise is contraindicated
  • Any upper or lower limb fracture in the last 6 months
  • Evidence of any surgical procedures in the knees, ankles, and hips or muscle damage in the last 6 months
  • Uncontrolled diabetes.
  • No able to speak and understand the Portuguese language
  • Refusal to give informed consent

Treatment and study plan

Dual task with variable- and fixed-priority instructions

Other

The participants were asked to perform dual-task activities focused, interchangeable or simultaneously, on balance (motor tasks) and on cognitive tasks performance, according to the instructional priority established by the physical therapist.

Dual-task with variable-priority instructions

Other

The participants were asked to spend half the session focused on balance (motor tasks) and half the session focused on cognitive tasks performance, according to the instructional priority established by the physical therapist.

Primary outcomes

  1. Gait spatiotemporal variables

    Time frame: Post-randomization at week 12

    These variables will be acquired by a couple of inertial sensors attached on participant's feet during walking on a 30-meter flat and level corridor under a single-task (only gait), dual-task under variable- (gait alternating with a cognitive task) and fixed-priority (gait and cognitive task performing simultaneously).

  2. Gait spatiotemporal variables

    Time frame: Post-randomization at week 24

    These variables will be acquired by a couple of inertial sensors attached on participant's feet during walking on a 30-meter flat and level corridor under a single-task (only gait), dual-task under variable- (gait alternating with a cognitive task) and fixed-priority (gait and cognitive task performing simultaneously).

  3. Gait spatiotemporal variables

    Time frame: Post-intervention at week 12

    These variables will be acquired by a couple of inertial sensors attached on participant's feet during walking on a 30-meter flat and level corridor under a single-task (only gait), dual-task under variable- (gait alternating with a cognitive task) and fixed-priority (gait and cognitive task performing simultaneously).

  4. Gait spatiotemporal variables

    Time frame: Post-intervention at week 24

    These variables will be acquired by a couple of inertial sensors attached on participant's feet during walking on a 30-meter flat and level corridor under a single-task (only gait), dual-task under variable- (gait alternating with a cognitive task) and fixed-priority (gait and cognitive task performing simultaneously).

Secondary outcomes

  1. Tri-axial acceleration, angular velocity, and displacement of the body center of mass during gait under single task

    Time frame: Post-randomization at week 12

    These biomechanical variable acquired during gait under single task will be assessed by an inertial sensor fixed on the participant's waist.

  2. Tri-axial acceleration, angular velocity, and displacement of the body center of mass during gait under single task

    Time frame: Post-radomization at week 24

    These biomechanical variable acquired during gait under single task will be assessed by an inertial sensor fixed on the participant's waist.

  3. Tri-axial acceleration, angular velocity, and displacement of the body center of mass during gait under single task

    Time frame: Post-intervention at week 12

    These biomechanical variable acquired during gait under single task will be assessed by an inertial sensor fixed on the participant's waist.

  4. Tri-axial acceleration, angular velocity, and displacement of the body center of mass during gait under single task

    Time frame: Post-intervention at week 24

    These biomechanical variable acquired during gait under single task will be assessed by an inertial sensor fixed on the participant's waist.

  5. Tri-axial acceleration, angular velocity and displacement of the body center of mass during gait under dual-task with variable-priority instruction

    Time frame: Post-randomization at week 12

    These biomechanical variable acquired during gait under dual-task with variable-priority instruction will be assessed by an inertial sensor fixed on the participant's waist.

  6. Tri-axial acceleration, angular velocity and displacement of the body center of mass during gait under dual-task with variable-priority instruction

    Time frame: Post-randomization at week 24

    These biomechanical variable acquired during gait under dual-task with variable-priority instruction will be assessed by an inertial sensor fixed on the participant's waist.

  7. Tri-axial acceleration, angular velocity and displacement of the body center of mass during gait under dual-task with variable-priority instruction

    Time frame: Post-intervention at week 12

    These biomechanical variable acquired during gait under dual-task with variable-priority instruction will be assessed by an inertial sensor fixed on the participant's waist.

  8. Tri-axial acceleration, angular velocity and displacement of the body center of mass during gait under dual-task with variable-priority instruction

    Time frame: Post-intervention at week 24

    These biomechanical variable acquired during gait under dual-task with variable-priority instruction will be assessed by an inertial sensor fixed on the participant's waist.

  9. Tri-axial acceleration, angular velocity and displacement of the body center of mass during gait under dual-task with fixed-priority instruction

    Time frame: Post-randomization at week 12

    These biomechanical variable acquired during gait under dual-task with fixed-priority instruction will be assessed by an inertial sensor fixed on the participant's waist.

  10. Tri-axial acceleration, angular velocity and displacement of the body center of mass during gait under dual-task with fixed-priority instruction

    Time frame: Post-randomization at week 24

    These biomechanical variable acquired during gait under dual-task with fixed-priority instruction will be assessed by an inertial sensor fixed on the participant's waist.

  11. Tri-axial acceleration, angular velocity and displacement of the body center of mass during gait under dual-task with fixed-priority instruction

    Time frame: Post-intervention at week 12

    These biomechanical variable acquired during gait under dual-task with fixed-priority instruction will be assessed by an inertial sensor fixed on the participant's waist.

  12. Tri-axial acceleration, angular velocity and displacement of the body center of mass during gait under dual-task with fixed-priority instruction

    Time frame: Post-intervention at week 24

    These biomechanical variable acquired during gait under dual-task with fixed-priority instruction will be assessed by an inertial sensor fixed on the participant's waist.

  13. Tri-axial acceleration, angular velocity and displacement of the body center of mass during conventional timed up and go test.

    Time frame: Post-randomization at week 12

    These biomechanical variable acquired during conventional timed up and go test will be assessed by an inertial sensor fixed on the participant's waist.

  14. Tri-axial acceleration, angular velocity and displacement of the body center of mass during conventional timed up and go test.

    Time frame: Post-randomization at week 24

    These biomechanical variable acquired during conventional timed up and go test will be assessed by an inertial sensor fixed on the participant's waist.

  15. Tri-axial acceleration, angular velocity and displacement of the body center of mass during conventional timed up and go test.

    Time frame: Post-intervention at week 12

    These biomechanical variable acquired during conventional timed up and go test will be assessed by an inertial sensor fixed on the participant's waist.

  16. Tri-axial acceleration, angular velocity and displacement of the body center of mass during conventional timed up and go test.

    Time frame: Post-intervention at week 24

    These biomechanical variable acquired during conventional timed up and go test will be assessed by an inertial sensor fixed on the participant's waist.

  17. Tri-axial acceleration, angular velocity, and displacement of the body center of mass during manual timed up and go test.

    Time frame: Post-randomization at week 12

    These biomechanical variable acquired during manual timed up and go test will be assessed by an inertial sensor fixed on the participant's waist.

  18. Tri-axial acceleration, angular velocity, and displacement of the body center of mass during manual timed up and go test.

    Time frame: Post-randomization at week 24

    These biomechanical variable acquired during manual timed up and go test will be assessed by an inertial sensor fixed on the participant's waist.

  19. Tri-axial acceleration, angular velocity, and displacement of the body center of mass during manual timed up and go test.

    Time frame: Post-intervention at week 12

    These biomechanical variable acquired during manual timed up and go test will be assessed by an inertial sensor fixed on the participant's waist.

  20. Tri-axial acceleration, angular velocity, and displacement of the body center of mass during manual timed up and go test.

    Time frame: Post-intervention at week 24

    These biomechanical variable acquired during manual timed up and go test will be assessed by an inertial sensor fixed on the participant's waist.

  21. Tri-axial acceleration, angular velocity, and displacement of the body center of mass during cognitive timed up and go test.

    Time frame: Post-randomization at week 12

    These biomechanical variable acquired during cognitive timed up and go test will be assessed by an inertial sensor fixed on the participant's waist.

  22. Tri-axial acceleration, angular velocity, and displacement of the body center of mass during cognitive timed up and go test.

    Time frame: Post-randomization at week 24

    These biomechanical variable acquired during cognitive timed up and go test will be assessed by an inertial sensor fixed on the participant's waist.

  23. Tri-axial acceleration, angular velocity, and displacement of the body center of mass during cognitive timed up and go test.

    Time frame: Post-intervention at week 12

    These biomechanical variable acquired during cognitive timed up and go test will be assessed by an inertial sensor fixed on the participant's waist.

  24. Tri-axial acceleration, angular velocity, and displacement of the body center of mass during cognitive timed up and go test.

    Time frame: Post-intervention at week 24

    These biomechanical variable acquired during cognitive timed up and go test will be assessed by an inertial sensor fixed on the participant's waist.

  25. Tri-axial acceleration, angular velocity, and displacement of the body center of mass during performing the Stroop test in quasi-static standing posture

    Time frame: Post-randomization at week 12

    These biomechanical variable acquired during performing the Stroop test in quasi-static standing posture will be assessed by an inertial sensor fixed on the participant's waist.

  26. Tri-axial acceleration, angular velocity, and displacement of the body center of mass during performing the Stroop test in quasi-static standing posture

    Time frame: Post-randomization at week 24

    These biomechanical variable acquired during performing the Stroop test in quasi-static standing posture will be assessed by an inertial sensor fixed on the participant's waist.

  27. Tri-axial acceleration, angular velocity, and displacement of the body center of mass during performing the Stroop test in quasi-static standing posture

    Time frame: Post-intervention at week 12

    These biomechanical variable acquired during performing the Stroop test in quasi-static standing posture will be assessed by an inertial sensor fixed on the participant's waist.

  28. Tri-axial acceleration, angular velocity, and displacement of the body center of mass during performing the Stroop test in quasi-static standing posture

    Time frame: Post-intervention at week 24

    These biomechanical variable acquired during performing the Stroop test in quasi-static standing posture will be assessed by an inertial sensor fixed on the participant's waist.

  29. Tri-axial acceleration, angular velocity and displacement of the body center of mass during performing the Clinical Test of Sensory Interaction and Balance (CTSIB).

    Time frame: Post-randomization at week 12

    These biomechanical variable acquired during performing the Clinical Test of Sensory Interaction and Balance (CTSIB) will be assessed by an inertial sensor fixed on the participant's waist.

  30. Tri-axial acceleration, angular velocity and displacement of the body center of mass during performing the Clinical Test of Sensory Interaction and Balance (CTSIB).

    Time frame: Post-randomization at week 24

    These biomechanical variable acquired during performing the Clinical Test of Sensory Interaction and Balance (CTSIB) will be assessed by an inertial sensor fixed on the participant's waist.

  31. Tri-axial acceleration, angular velocity and displacement of the body center of mass during performing the Clinical Test of Sensory Interaction and Balance (CTSIB).

    Time frame: Post-intervention at week 12

    These biomechanical variable acquired during performing the Clinical Test of Sensory Interaction and Balance (CTSIB) will be assessed by an inertial sensor fixed on the participant's waist.

  32. Tri-axial acceleration, angular velocity and displacement of the body center of mass during performing the Clinical Test of Sensory Interaction and Balance (CTSIB).

    Time frame: Post-intervention at week 24

    These biomechanical variable acquired during performing the Clinical Test of Sensory Interaction and Balance (CTSIB) will be assessed by an inertial sensor fixed on the participant's waist.

  33. Tri-axial acceleration, angular velocity, and displacement of the body center of mass during performing the Anterior Functional Reach test.

    Time frame: Post-randomization at week 12

    These biomechanical variable acquired during performing the Anterior Functional Reach test will be assessed by an inertial sensor fixed on the participant's waist.

  34. Tri-axial acceleration, angular velocity, and displacement of the body center of mass during performing the Anterior Functional Reach test.

    Time frame: Post-randomization at week 24

    These biomechanical variable acquired during performing the Anterior Functional Reach test will be assessed by an inertial sensor fixed on the participant's waist.

  35. Tri-axial acceleration, angular velocity, and displacement of the body center of mass during performing the Anterior Functional Reach test.

    Time frame: Post-intervention at week 12

    These biomechanical variable acquired during performing the Anterior Functional Reach test will be assessed by an inertial sensor fixed on the participant's waist.

  36. Tri-axial acceleration, angular velocity, and displacement of the body center of mass during performing the Anterior Functional Reach test.

    Time frame: Post-intervention at week 24

    These biomechanical variable acquired during performing the Anterior Functional Reach test will be assessed by an inertial sensor fixed on the participant's waist.

  37. Tri-axial acceleration, angular velocity, and displacement of the body center of mass during performing the Five Times Sit-to-stand test from a chair.

    Time frame: Post-randomization at week 12

    These biomechanical variable acquired during performing the Five Times Sit-to-stand test from a chair will be assessed by an inertial sensor fixed on the participant's waist.

  38. Tri-axial acceleration, angular velocity, and displacement of the body center of mass during performing the Five Times Sit-to-stand test from a chair.

    Time frame: Post-randomization at week 24

    These biomechanical variable acquired during performing the Five Times Sit-to-stand test from a chair will be assessed by an inertial sensor fixed on the participant's waist.

  39. Tri-axial acceleration, angular velocity, and displacement of the body center of mass during performing the Five Times Sit-to-stand test from a chair.

    Time frame: Post-intervention at week 12

    These biomechanical variable acquired during performing the Five Times Sit-to-stand test from a chair will be assessed by an inertial sensor fixed on the participant's waist.

  40. Tri-axial acceleration, angular velocity, and displacement of the body center of mass during performing the Five Times Sit-to-stand test from a chair.

    Time frame: Post-intervention at week 24

    These biomechanical variable acquired during performing the Five Times Sit-to-stand test from a chair will be assessed by an inertial sensor fixed on the participant's waist.

  41. Tri-axial acceleration, angular velocity, and displacement of the body center of mass during performing the Sitting-rising test from the floor.

    Time frame: Post-randomization at week 12

    These biomechanical variable acquired during performing the Sitting-rising test from the floor will be assessed by an inertial sensor fixed on the participant's waist.

  42. Tri-axial acceleration, angular velocity, and displacement of the body center of mass during performing the Sitting-rising test from the floor.

    Time frame: Post-randomization at week 24

    These biomechanical variable acquired during performing the Sitting-rising test from the floor will be assessed by an inertial sensor fixed on the participant's waist.

  43. Tri-axial acceleration, angular velocity, and displacement of the body center of mass during performing the Sitting-rising test from the floor.

    Time frame: Post-intervention at week 12

    These biomechanical variable acquired during performing the Sitting-rising test from the floor will be assessed by an inertial sensor fixed on the participant's waist.

  44. Tri-axial acceleration, angular velocity, and displacement of the body center of mass during performing the Sitting-rising test from the floor.

    Time frame: Post-intervention at week 24

    These biomechanical variable acquired during performing the Sitting-rising test from the floor will be assessed by an inertial sensor fixed on the participant's waist.

  45. Timed Up and Go conventional (TUG conventional)

    Time frame: Post-randomization at week 12

    Test of basic mobility skills analyzed during rising from a chair, walking, turning the obstacle, and sitting again on the chair.

  46. Timed Up and Go conventional (TUG conventional)

    Time frame: Post-randomization at week 24

    Test of basic mobility skills analyzed during rising from a chair, walking, turning the obstacle, and sitting again on the chair.

  47. Timed Up and Go conventional (TUG conventional)

    Time frame: Post-intervention at week 12

    Test of basic mobility skills analyzed during rising from a chair, walking, turning the obstacle, and sitting again on the chair.

  48. Timed Up and Go conventional (TUG conventional)

    Time frame: Post-intervention at week 24

    Test of basic mobility skills analyzed during rising from a chair, walking, turning the obstacle, and sitting again on the chair.

  49. Timed Up and Go manual (TUG manual)

    Time frame: Post-randomization at week 12

    Test of basic mobility skills analyzed during rising from a chair, walking, turning the obstacle, and sitting again on the chair, while the participant carries a dish with a cup on it.

  50. Timed Up and Go manual (TUG manual)

    Time frame: Post-randomization at week 24

    Test of basic mobility skills analyzed during rising from a chair, walking, turning the obstacle, and sitting again on the chair, while the participant carries a dish with a cup on it.

  51. Timed Up and Go manual (TUG manual)

    Time frame: Post-intervention at week 12

    Test of basic mobility skills analyzed during rising from a chair, walking, turning the obstacle, and sitting again on the chair, while the participant carries a dish with a cup on it.

  52. Timed Up and Go manual (TUG manual)

    Time frame: Post-intervention at week 24

    Test of basic mobility skills analyzed during rising from a chair, walking, turning the obstacle, and sitting again on the chair, while the participant carries a dish with a cup on it.

  53. Timed Up and Go cognitive (TUG cognitive)

    Time frame: Post-randomization at week 12

    Test the basic mobility skills analyzed during raising from a chair, walking, bypassing the obstacle, and sitting back in the chair while the participant performs a concurrent cognitive task (solving mathematical subtraction operations).

  54. Timed Up and Go cognitive (TUG cognitive)

    Time frame: Post-randomization at week 24

    Test the basic mobility skills analyzed during raising from a chair, walking, bypassing the obstacle, and sitting back in the chair while the participant performs a concurrent cognitive task (solving mathematical subtraction operations).

  55. Timed Up and Go cognitive (TUG cognitive)

    Time frame: Post-intervention at week 12

    Test the basic mobility skills analyzed during raising from a chair, walking, bypassing the obstacle, and sitting back in the chair while the participant performs a concurrent cognitive task (solving mathematical subtraction operations).

  56. Timed Up and Go cognitive (TUG cognitive)

    Time frame: Post-intervention at week 24

    Test the basic mobility skills analyzed during raising from a chair, walking, bypassing the obstacle, and sitting back in the chair while the participant performs a concurrent cognitive task (solving mathematical subtraction operations).

  57. Postural Balance Test (PBT)

    Time frame: Post-randomization at week 12

    The Postural Balance Test evaluate the static and dynamic balance, in order to verify the typology of motor regulation, i.e. the exteroceptive or visual (six items) and interoceptive or vestibular (eight items), besides the general - proprioceptive information - of the movements.

  58. Postural Balance Test (PBT)

    Time frame: Post-randomization at week 24

    The Postural Balance Test evaluate the static and dynamic balance, in order to verify the typology of motor regulation, i.e. the exteroceptive or visual (six items) and interoceptive or vestibular (eight items), besides the general - proprioceptive information - of the movements.

  59. Postural Balance Test (PBT)

    Time frame: Post-intervention at week 12

    The Postural Balance Test evaluate the static and dynamic balance, in order to verify the typology of motor regulation, i.e. the exteroceptive or visual (six items) and interoceptive or vestibular (eight items), besides the general - proprioceptive information - of the movements.

  60. Postural Balance Test (PBT)

    Time frame: Post-intervention at week 24

    The Postural Balance Test evaluate the static and dynamic balance, in order to verify the typology of motor regulation, i.e. the exteroceptive or visual (six items) and interoceptive or vestibular (eight items), besides the general - proprioceptive information - of the movements.

  61. Clinical Test of Sensory Interaction and Balance (CTSIB)

    Time frame: Post-randomization at week 12

    This test will be used to assess the sensory integration on postural balance during standing on a stable and unstable surface with eyes open and closed.

  62. Clinical Test of Sensory Interaction and Balance (CTSIB)

    Time frame: Post-randomization at week 24

    This test will be used to assess the sensory integration on postural balance during standing on a stable and unstable surface with eyes open and closed.

  63. Clinical Test of Sensory Interaction and Balance (CTSIB)

    Time frame: Post-intervention at week 12

    This test will be used to assess the sensory integration on postural balance during standing on a stable and unstable surface with eyes open and closed.

  64. Clinical Test of Sensory Interaction and Balance (CTSIB)

    Time frame: Post-intervention at week 24

    This test will be used to assess the sensory integration on postural balance during standing on a stable and unstable surface with eyes open and closed.

  65. Stroop test in sit posture

    Time frame: Post-randomization at week 12

    This test will be used to measure a participant's selective attention capacity and skills, as well as his/her processing speed ability in sit posture

  66. Stroop test in sit posture

    Time frame: Post-randomization at week 24

    This test will be used to measure a participant's selective attention capacity and skills, as well as his/her processing speed ability in sit posture

  67. Stroop test in sit posture

    Time frame: Post-intervention at week 12

    This test will be used to measure a participant's selective attention capacity and skills, as well as his/her processing speed ability in sit posture

  68. Stroop test in a quasi-static standing posture

    Time frame: Post-intervention at week 24

    This test will be used to measure a participant's selective attention capacity and skills, as well as his/her processing speed ability in quasi-static standing posture.

  69. Trail making test (TMT)

    Time frame: Post-randomization at week 12

    Trail making test will be used to assess the participants executive abilities, which requires a variety of mental abilities including letter and number recognition mental flexibility, visual scanning, and motor function of upper limbs

  70. Trail making test (TMT)

    Time frame: Post-randomization at week 24

    Trail making test will be used to assess the participants executive abilities, which requires a variety of mental abilities including letter and number recognition mental flexibility, visual scanning, and motor function of upper limbs

  71. Trail making test (TMT)

    Time frame: Post-intervention at week 12

    Trail making test will be used to assess the participants executive abilities, which requires a variety of mental abilities including letter and number recognition mental flexibility, visual scanning, and motor function of upper limbs

  72. Trail making test (TMT)

    Time frame: Post-intervention at week 24

    Trail making test will be used to assess the participants executive abilities, which requires a variety of mental abilities including letter and number recognition mental flexibility, visual scanning, and motor function of upper limbs

  73. Five Times Sit-to-Stand test from a chair

    Time frame: Post-randomization at week 12

    The functional performance of the lower limbs taken to lifting and sitting on a chair for five times. The time will be measured by a stopwatch

  74. Five Times Sit-to-Stand test from a chair

    Time frame: Post-randomization at week 24

    The functional performance of the lower limbs taken to lifting and sitting on a chair for five times. The time will be measured by a stopwatch

  75. Five Times Sit-to-Stand test from a chair

    Time frame: Post-intervention at week 12

    The functional performance of the lower limbs taken to lifting and sitting on a chair for five times. The time will be measured by a stopwatch

  76. Five Times Sit-to-Stand test from a chair

    Time frame: Post-intervention at week 24

    The functional performance of the lower limbs taken to lifting and sitting on a chair for five times. The time will be measured by a stopwatch

  77. Sitting-and-rising test from the floor

    Time frame: Post-randomization at week 12

    Sitting-and-rising test from the floor will be used to quantify how many supports (hands and/or knees or, still, hands on the knees or legs) the individual uses to sit and lift from the floor.

  78. Sitting-and-rising test from the floor

    Time frame: Post-randomization at week 24

    Sitting-and-rising test from the floor will be used to quantify how many supports (hands and/or knees or, still, hands on the knees or legs) the individual uses to sit and lift from the floor.

  79. Sitting-and-rising test from the floor

    Time frame: Post-intervention at week 12

    Sitting-and-rising test from the floor will be used to quantify how many supports (hands and/or knees or, still, hands on the knees or legs) the individual uses to sit and lift from the floor.

  80. Sitting-and-rising test from the floor

    Time frame: Post-intervention at week 24

    Sitting-and-rising test from the floor will be used to quantify how many supports (hands and/or knees or, still, hands on the knees or legs) the individual uses to sit and lift from the floor.

  81. Anterior functional reach test

    Time frame: Post-randomization at week 12

    Anterior functional reach test will be used to determine how far the participants are able to move forward within their stability limit. It is widely used to identify the risk of falling in older adults

  82. Anterior functional reach test

    Time frame: Post-randomization at week 24

    Anterior functional reach test will be used to determine how far the participants are able to move forward within their stability limit. It is widely used to identify the risk of falling in older adults

  83. Anterior functional reach test

    Time frame: Post-intervention at week 12

    Anterior functional reach test will be used to determine how far the participants are able to move forward within their stability limit. It is widely used to identify the risk of falling in older adults

  84. Anterior functional reach test

    Time frame: Post-intervention at week 24

    Anterior functional reach test will be used to determine how far the participants are able to move forward within their stability limit. It is widely used to identify the risk of falling in older adults

  85. Falls Efficacy Scale-International (FES-I)

    Time frame: Post-randomization at week 12

    The 16-item Falls Efficacy Scale-International will be used to measure the participant's fear of falling (the concerns about falling). The sum of all 16 items is considered to compute a total score. The higher the total score achieved by the participant, the higher the concerns about falling.

  86. Falls Efficacy Scale-International (FES-I)

    Time frame: Post-randomization at week 24

    The 16-item Falls Efficacy Scale-International will be used to measure the participant's fear of falling (the concerns about falling). The sum of all 16 items is considered to compute a total score. The higher the total score achieved by the participant, the higher the concerns about falling.

  87. Falls Efficacy Scale-International (FES-I)

    Time frame: Post-intervention at week 12

    The 16-item Falls Efficacy Scale-International will be used to measure the participant's fear of falling (the concerns about falling). The sum of all 16 items is considered to compute a total score. The higher the total score achieved by the participant, the higher the concerns about falling.

  88. Falls Efficacy Scale-International (FES-I)

    Time frame: Post-intervention at week 24

    The 16-item Falls Efficacy Scale-International will be used to measure the participant's fear of falling (the concerns about falling). The sum of all 16 items is considered to compute a total score. The higher the total score achieved by the participant, the higher the concerns about falling.

  89. Activities-specific Balance Confidence (ABC Scale)

    Time frame: Post-randomization at week 12

    The 16-item Activities-specific Balance Confidence Scale will be used to measure the level of balance confidence of the individual during the accomplishment in performing daily activities. The higher the total score achieved by the participant, the higher the level of balance confidence and functioning in daily activities

  90. Activities-specific Balance Confidence (ABC Scale)

    Time frame: Post-randomization at week 24

    The 16-item Activities-specific Balance Confidence Scale will be used to measure the level of balance confidence of the individual during the accomplishment in performing daily activities. The higher the total score achieved by the participant, the higher the level of balance confidence and functioning in daily activities

  91. Activities-specific Balance Confidence (ABC Scale)

    Time frame: Post-intervention at week 12

    The 16-item Activities-specific Balance Confidence Scale will be used to measure the level of balance confidence of the individual during the accomplishment in performing daily activities. The higher the total score achieved by the participant, the higher the level of balance confidence and functioning in daily activities

  92. Activities-specific Balance Confidence (ABC Scale)

    Time frame: Post-intervention at week 24

    The 16-item Activities-specific Balance Confidence Scale will be used to measure the level of balance confidence of the individual during the accomplishment in performing daily activities. The higher the total score achieved by the participant, the higher the level of balance confidence and functioning in daily activities

  93. Medical Outcomes Study 36-Item Short-Form Health Survey (SF-36)

    Time frame: Post-randomization at week 12

    Medical Outcomes Study 36-Item Short-Form Health Survey will be used to evaluate the quality of life of the participants. The SF-36 consists of eight scaled scores, which are the weighted sums of the questions in their section. Each scale is directly transformed into a 0-100 scale on the assumption that each question carries equal weight. The lower the score the more disability. The higher the score the less disability i.e., a score of zero is equivalent to maximum disability and a score of 100 is equivalent to no disability

  94. Medical Outcomes Study 36-Item Short-Form Health Survey (SF-36)

    Time frame: Post-randomization at week 24

    Medical Outcomes Study 36-Item Short-Form Health Survey will be used to evaluate the quality of life of the participants. The SF-36 consists of eight scaled scores, which are the weighted sums of the questions in their section. Each scale is directly transformed into a 0-100 scale on the assumption that each question carries equal weight. The lower the score the more disability. The higher the score the less disability i.e., a score of zero is equivalent to maximum disability and a score of 100 is equivalent to no disability

  95. Medical Outcomes Study 36-Item Short-Form Health Survey (SF-36)

    Time frame: Post-intervention at week 12

    Medical Outcomes Study 36-Item Short-Form Health Survey will be used to evaluate the quality of life of the participants. The SF-36 consists of eight scaled scores, which are the weighted sums of the questions in their section. Each scale is directly transformed into a 0-100 scale on the assumption that each question carries equal weight. The lower the score the more disability. The higher the score the less disability i.e., a score of zero is equivalent to maximum disability and a score of 100 is equivalent to no disability

  96. Medical Outcomes Study 36-Item Short-Form Health Survey (SF-36)

    Time frame: Post-intervention at week 24

    Medical Outcomes Study 36-Item Short-Form Health Survey will be used to evaluate the quality of life of the participants. The SF-36 consists of eight scaled scores, which are the weighted sums of the questions in their section. Each scale is directly transformed into a 0-100 scale on the assumption that each question carries equal weight. The lower the score the more disability. The higher the score the less disability i.e., a score of zero is equivalent to maximum disability and a score of 100 is equivalent to no disability

  97. Short form of the Geriatric Depression Scale (GDS-15)

    Time frame: Post-randomization at week 12

    This 15-item instrument will be used to evaluate the suggestive depression symptoms in the participants. Its items require a yes/no response. Answers indicating depression are in bold and italicized; score one point for each one selected. Each answer "yes" marked with X in questions 3, 4, 6, 8, 9, 10, 12, 14 and 15 or answer "no" noted in questions 1, 5, 7, 11 and 13, computes 1 point. A score of 0 to 5 is normal. A score greater than 5 indicates depression

  98. Short form of the Geriatric Depression Scale (GDS-15)

    Time frame: Post-randomization at week 24

    This 15-item instrument will be used to evaluate the suggestive depression symptoms in the participants. Its items require a yes/no response. Answers indicating depression are in bold and italicized; score one point for each one selected. Each answer "yes" marked with X in questions 3, 4, 6, 8, 9, 10, 12, 14 and 15 or answer "no" noted in questions 1, 5, 7, 11 and 13, computes 1 point. A score of 0 to 5 is normal. A score greater than 5 indicates depression

  99. Short form of the Geriatric Depression Scale (GDS-15)

    Time frame: Post-intervention at week 12

    This 15-item instrument will be used to evaluate the suggestive depression symptoms in the participants. Its items require a yes/no response. Answers indicating depression are in bold and italicized; score one point for each one selected. Each answer "yes" marked with X in questions 3, 4, 6, 8, 9, 10, 12, 14 and 15 or answer "no" noted in questions 1, 5, 7, 11 and 13, computes 1 point. A score of 0 to 5 is normal. A score greater than 5 indicates depression

  100. Short form of the Geriatric Depression Scale (GDS-15)

    Time frame: Post-intervention at week 24

    This 15-item instrument will be used to evaluate the suggestive depression symptoms in the participants. Its items require a yes/no response. Answers indicating depression are in bold and italicized; score one point for each one selected. Each answer "yes" marked with X in questions 3, 4, 6, 8, 9, 10, 12, 14 and 15 or answer "no" noted in questions 1, 5, 7, 11 and 13, computes 1 point. A score of 0 to 5 is normal. A score greater than 5 indicates depression

  101. The falls events

    Time frame: Post-randomization at week 12

    Fall events will be evaluated through a falls diary, delivered monthly by each participant. The participants should note in this diary the day and the fall causes and circumstances.

  102. The falls events

    Time frame: Post-randomization at week 24

    Fall events will be evaluated through a falls diary, delivered monthly by each participant. The participants should note in this diary the day and the fall causes and circumstances.

  103. The falls events

    Time frame: Post-intervention at week 12

    Fall events will be evaluated through a falls diary, delivered monthly by each participant. The participants should note in this diary the day and the fall causes and circumstances.

  104. The falls events

    Time frame: Post-intervention at week 24

    Fall events will be evaluated through a falls diary, delivered monthly by each participant. The participants should note in this diary the day and the fall causes and circumstances.

Sponsors and collaborators

Lead sponsor

University of Pernambuco

Other

Collaborators

  • Conselho Nacional de Desenvolvimento Científico e Tecnológico

Registry information

Official study title

The Effectiveness of Dual-task Training With Variable- and Fixed-priority Instructions on Gait Speed in Community-dwelling Older Adults

Important dates

Study start
2019
Primary completion
2020
Study completion
2020
First posted
Mar 22, 2019
Registry last updated
Jul 21, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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