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Clinical Trials in Turkey / NCT07468968
Enrolling by invitation Not applicable

Comparative Effects of Balance and Inspiratory Muscle Training in Older Adults

NCT07468968 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-03-12
Last updated
2026-03-18

Condition(s) studied

GeriatricGeriatrics RehabilitationGeriatric FallGeriatric Health

Investigational drug(s) / intervention(s)

Inspiratory Muscle TrainingBalance Training

Inspiratory Muscle Training: 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.

Balance Training: 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.

Study summary

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.

Eligibility

Sex
ALL
Min age
60 Years
Max age
—
Healthy volunteers
No
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.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Darülaceze Müdürlüğü Istanbul Turkey (Türkiye)

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07468968 on ClinicalTrials.gov ↗ ← All trials in Turkey