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NCT Number: NCT07468968

Comparative Effects of Balance and Inspiratory Muscle Training in Older Adults

This study aims to investigate and compare the effects of Inspiratory Muscle Training (IMT), balance training, and a combination of both on respiratory muscle strength and balance in older adults. Aging is often associated with a decline in skeletal and respiratory muscle strength, which can increase the risk of falls and impact overall functionality.

Participants aged 60 and over will be randomly assigned to one of three groups:

Respiratory Muscle Training group (30 breaths, twice daily),

Balance Training group (45-50 minute sessions, 3 days a week),

Combined Training group (both IMT and balance exercises).

The intervention will last for 8-weeks. Researchers will evaluate respiratory muscle strength, balance, core endurance, and functional capacity before and after the 8-week program to determine which approach is most effective in improving these parameters in the geriatric population.

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Key information

Age range

60 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Darülaceze Müdürlüğü

Istanbul, Turkey (Türkiye)

About this study

This is a 3-arm randomized comparative trial designed to evaluate the synergistic effects of respiratory and physical interventions in the geriatric population. Physiological changes due to aging, such as reduced inspiratory muscle pressure (MIP) and impaired postural control, are closely linked to increased mortality and fall risk. This study tests the hypothesis that combining IMT with balance training will yield superior outcomes compared to single-mode interventions.

Methodology and Interventions:

Participants will be allocated into three groups using block randomization to ensure gender balance (n=12 per group, total target n=36, accounting for a 20% potential attrition rate):

Group 1 (IMT): Participants will perform 30 breaths twice daily using an IMT device for 8 weeks.

Group 2 (Balance): Participants will attend 45-50 minute supervised balance training sessions, 3 days per week for 8 weeks.

Group 3 (Combined): Participants will perform both the daily IMT protocol and the thrice-weekly balance sessions.

Evaluation Criteria:

Outcomes will be measured at baseline and after the 8-week intervention. Primary outcomes include Maximal Inspiratory Pressure (MIP), Maximal Expiratory Pressure (MEP), Timed Up and Go (TUG) test, Short Physical Performance Battery (SPPB), 6-Minute Walk Test (6MWT), core endurance tests, and single-leg stance balance.

Data from participants who complete at least 70% of the training sessions will be included in the final analysis. The study aims to provide evidence-based recommendations for enhancing functional independence and reducing fall risk in older adults.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Aged 60 years or older.
  • Mini-Mental State Examination (MMSE) score of 22 or higher.
  • Ability to walk 10 meters independently without human assistance.
  • Ability to read and write.
  • Volunteering to participate and providing written informed consent.

Exclusion criteria

  • Current use of sedative or hypnotic medications.
  • Presence of a diagnosed neurological disorder (e.g., history of stroke, Parkinson's disease, Multiple Sclerosis, dementia, or clinical vertigo) that is currently under treatment.
  • Presence of clinically significant cardiovascular or pulmonary complications (e.g., COPD, active lung disease, or uncontrolled hypertension).
  • Severe postural abnormalities that may interfere with the study (e.g., advanced scoliosis or kyphosis).
  • Acute or chronic orthopedic conditions preventing participation in a balance exercise program (e.g., lower extremity fractures or severe joint instability).
  • High risk of sarcopenia, defined as a SARC-F score of 4 or higher.
  • Significant communication or cognitive barriers that prevent following the exercise instructions.

Treatment and study plan

Inspiratory muscle training

Device

Participants will use a threshold inspiratory muscle trainer device. The training involves performing 30 breaths twice a day (morning and evening), 7 days a week for 8 consecutive weeks. The resistance (intensity) will be adjusted based on the participant's maximal inspiratory pressure (MIP) to ensure progressive training.

Other names: Threshold IMT, Respiratory Muscle Training.

Balance training

Behavioral

A structured balance training program conducted under the supervision of a therapist. Sessions last 45-50 minutes, held 3 days per week for 8 weeks. The program includes static and dynamic balance exercises, weight-shifting tasks, and functional movement patterns designed to reduce fall risk.

Primary outcomes

  1. Maximal Inspiratory Pressure (MIP)

    Time frame: Baseline and 8 weeks.

    MIP will be measured using a digital pressure gauge to evaluate the strength of the inspiratory muscles. The best of three maneuvers will be recorded in cmH2O. Higher values indicate better respiratory muscle strength.

  2. Maximal Expiratory Pressure (MEP)

    Time frame: Baseline and 8 weeks.

    MEP will be measured using a digital pressure gauge to evaluate the strength of the expiratory muscles. The best of three maneuvers will be recorded in cmH2O. Higher values indicate better expiratory muscle strength.

  3. Timed Up and Go (TUG) Test

    Time frame: Baseline and 8 weeks.

    The TUG test measures the time (in seconds) it takes for a participant to stand up from a chair, walk 3 meters, turn around, walk back, and sit down. Lower scores (less time) indicate better functional mobility and balance.

  4. Respiratory Muscle Endurance (Incremental Threshold Loading Test)

    Time frame: Baseline and 8 weeks.

    Respiratory muscle endurance will be assessed using an incremental threshold loading test (ITLT). The test starts with an initial load based on the participant's Maximal Inspiratory Pressure (MIP). The resistance is increased by 20% of the initial MIP value every 2 minutes. Participants are instructed to maintain their breathing pattern against the increasing load until exhaustion or until they can no longer overcome the threshold. The total duration (in seconds) sustained during the test is recorded. Higher values indicate better respiratory muscle endurance.

  5. Single Leg Stance Test (SLST)

    Time frame: Baseline and 8 weeks.

    The participant stands on one leg for as long as possible without support. The time (in seconds) until balance is lost is recorded (up to a maximum of 30 or 60 seconds). Higher values indicate better static balance.

  6. 6-Minute Walk Test (6MWT)

    Time frame: Baseline and 8 weeks.

    The 6MWT measures the total distance (in meters) a participant can walk on a flat, hard surface in a period of 6 minutes. It is used to assess submaximal functional exercise capacity.

  7. Core Muscle Endurance Test

    Time frame: Baseline and 8 weeks.

    Core endurance will be assessed using static holding test (McGill's torso endurance test). The duration (in seconds) the participant can maintain the position is recorded. Higher duration indicates better core stability.

Secondary outcomes

  1. Short Physical Performance Battery (SPPB)

    Time frame: Baseline and 8 weeks.

    SPPB consists of three components: standing balance, gait speed, and chair stand tests. Each component is scored from 0 to 4, with a total score ranging from 0 to 12. Higher scores indicate better physical performance.

  2. Charlson Comorbidity Index (CCI)

    Time frame: Baseline.

    This index categorizes or weights comorbid conditions to predict the 10-year survival for patients. The scores are summed to provide a total score (0 to 37). Higher scores indicate a higher burden of comorbidity and a lower 10-year survival probability.

  3. Mini-Mental State Examination (MMSE)

    Time frame: Baseline.

    A 30-point questionnaire used extensively in clinical and research settings to measure cognitive impairment. Scores range from 0 to 30. Higher scores indicate better cognitive function.

  4. Montreal Cognitive Assessment (MoCA)

    Time frame: Baseline.

    A rapid screening instrument for mild cognitive dysfunction. It assesses different cognitive domains: attention and concentration, executive functions, memory, language, visuoconstructional skills, conceptual thinking, calculations, and orientation. Total score is 30. Higher scores indicate better cognitive performance.

  5. Tinetti Performance-Oriented Mobility Assessment (POMA)

    Time frame: Baseline and 8 weeks.

    A task-oriented test that measures an older adult's gait and balance abilities. The maximum score is 28, with 16 points for balance and 12 for gait. Higher scores indicate better mobility and lower fall risk.

  6. Handgrip Strength

    Time frame: Baseline and 8 weeks.

    Handgrip strength will be measured in kilograms (kg) using a calibrated handheld dynamometer. Participants will perform three trials with their dominant hand, and the maximum value will be recorded. Higher values indicate better upper extremity muscle strength.

  7. Physical Activity Scale for the Elderly (PASE)

    Time frame: Baseline.

    A brief instrument to assess physical activity in older adults. It scores occupational, household, and leisure activities over a one-week period. Higher scores indicate a higher level of physical activity.

  8. Fatigue Impact Scale (FIS)

    Time frame: Baseline.

    A self-reported questionnaire that measures the impact of fatigue on daily functioning and quality of life. Higher scores indicate a greater impact of fatigue on the individual's life.

Sponsors and collaborators

Lead sponsor

Acibadem University

Other

Collaborators

  • Biruni University

Registry information

Official study title

Comparative Effects of Balance and Inspiratory Muscle Training on Balance, Respiratory Muscle Strength, and Physical Performance in Older Adults: A Randomized Comparative Trial

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Mar 13, 2026
Registry last updated
Mar 18, 2026

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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