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Completed

NCT Number: NCT05765552

Effects of Dual-Task Training In Individuals With Alzheimer

The purpose of this study is to investigate the effects of dual-task training on balance, fear of falling, cognitive functions, dual-task performance, depression and quality of life in individuals with Alzheimer.

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Key information

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Karsiyaka Municipality Day Living Center

Izmir, Karsıyaka, 35580, Turkey (Türkiye)

About this study

Eligible participants will be randomized to control or dual-task training group.Control group will receive conventional therapy generally consisted of lower and upper range of motion exercises for 30 minutes 2 times a week for 8 weeks.Dual-task training group will receive exercises involving motor-cognitive dual-task exercises for 30 minutes 2 times a week for 8 weeks.Each participant will be assessed before and after the 8 weeks of treatment.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • having been diagnosed with mild or moderate Alzheimer's disease
  • able to walk with or without assistance
  • having sufficient visual and auditory ability to perform the cognitive tests
  • being fit to perform physical exercises
  • being able to participate in proposed interventions and assessments

Exclusion criteria

  • having a neurological disorder other than Alzheimer
  • having any musculoskeletal problems that can affect balance
  • having any contraindication to exercise
  • functional limitation or sensory impairment that may affect performance
  • major depression

Treatment and study plan

Dual-Task Training

Other

Motor-cognitive dual-task exercises will be applied for 2 days a week for 8 weeks.Sessions will last for 30 minutes.

Control Group

Other

Upper and lower extremity range of motion exercises will be applied for 8-10 repetitions for 1 set 2 times a week for 8 weeks.

Primary outcomes

  1. Timed Up And Go(TUG)

    Time frame: eight weeks

    It is a frequently used test that evaluates functional mobility and dynamic balance. At the beginning of the test, individuals sit in a chair. A distance of 3 m is set in front of the patient. With the start command, the patient gets up from his seat and walks 3 m, turns around and walks back and sits. With the start command, the time until the moment of sitting on the chair is recorded in seconds.Shorter duration indicates better functional mobility.

  2. 5 Times Sit To Stand Test(5XSST)

    Time frame: eight weeks

    5XSST evaluates lower extremity functional strength, transitional movements, balance and fall risk. The time it takes for the participant to sit and get up from a chair 5 times is recorded in seconds. Interpretations are made about balance and fall risk by comparing the norm times for age with the time the individual completes the test.

  3. Cognitive Reserve Index Questionaire(CRIq)

    Time frame: eight weeks

    CRIq assesses an individual's cognitive reserve through compiling information about their entire adult life. If the participant has a suspected or confirmed cognitive weakness, the questionnaire must be answered by a family member or caregiver. The total score is obtained by recording the frequency of the individual's educational life, work and leisure activities in years. According to the score, the participant's cognitive reserve is interpreted as low, low - medium, medium, medium - high or high

  4. Quality of Life in Alzheimer's Disease(QOL-AD)

    Time frame: eight weeks

    There are two versions of the scale: patient and family member/caregiver. In order to maximize construct validity, the scale is filled in independently by both patients and caregivers. It consists of questions asked about different aspects of life in order to determine the quality of life of the person. For each question, they are asked to choose the most appropriate one from the Poor, Fair, Good or Excellent answers.Higher scores indicate better quality of life.

  5. Geriatric Depression Scale(GDS)

    Time frame: eight weeks

    The scale consists of 30 questions questioning how the participant felt in the past week. The person is asked to give the appropriate Yes(0) or No(1) answer to each question.Scores higher than 5 indicate depression.

Secondary outcomes

  1. Dual-Task Questionnaire(DTQ)

    Time frame: eight weeks

    The Dual Task Questionnaire assesses the frequency of difficulties experienced by individuals with neurological injury or disease during activities of daily living that involve dual tasks. DTQ is scored between 0-40. Higher scores indicate more frequent dual-task difficulties.

  2. Modified Falling Efficacy Scale(MFES)

    Time frame: eight weeks

    The scale consists of 14 items. On a scale of 0 to 10 (on the scale), the participant asked how safe they feel doing each of these activities without falling, with 0 being "not safe/not sure", 5 "quite safe/quite confident", and 10 "completely safe/ are asked to rate it in terms of being completely sure.

  3. Mini Mental Test(MMT)

    Time frame: eight weeks

    Scoring is made between 0-30 on the scale in which the sub-headings of orientation, recording memory, attention and calculation, recall, language are evaluated.Lesser scores indicate worse cognitive function.

Sponsors and collaborators

Lead sponsor

Ege University

Other

Registry information

Official study title

Effects Of Dual-Task Training On Balance, Fear Of Falling,Cognitive Functions, Dual-Task Performance, Depression And Quality Of Life In Individuals With Alzheimer

Important dates

Study start
2023
Primary completion
2023
Study completion
2024
First posted
Mar 13, 2023
Registry last updated
Nov 20, 2025

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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