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Functional and Physiological Responses to Multicomponent Exercise in Older Adults

Functional and Physiological Responses to a 12-Week Multicomponent Exercise Program in Older Adults: An Exploratory Responder-Non-Responder Analysis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07702227
Enrollment
40
Registered
2026-07-14
Start date
2026-06-01
Completion date
2026-09-30
Last updated
2026-07-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Aging, Exercise Response, Functional Capacity, Heart Rate Variability (HRV), Older Adults (60 - 85 Years Old)

Keywords

heart rate variability, cardiac autonomic function, multicomponent exercise, six-minute walk test, responder non-responder

Brief summary

This study will examine functional and physiological responses to a 12-week multicomponent exercise program in community-dwelling older adults. Adults aged 60 to 81 years will be randomly assigned to either a multicomponent exercise group or a control group. The supervised exercise program will be performed twice weekly for 12 weeks and will include aerobic walking, resistance exercises, balance and agility training, flexibility exercises, and cool-down activities. Functional performance will be assessed using the six-minute walk test, the 30-second chair stand test, and the 8-Foot Up and Go test at baseline and after 12 weeks. Resting cardiac autonomic function will be assessed using heart rate variability. In addition, an exploratory responder-non-responder analysis will be conducted to examine whether baseline heart rate variability is associated with individual functional adaptations following the exercise program. This study may help identify physiological markers related to functional responsiveness to exercise in older adults.

Interventions

Participants in the exercise group will complete a supervised multicomponent exercise program twice weekly for 12 weeks. Each session will last approximately 45 to 50 minutes and include warm-up, aerobic interval walking, resistance exercises, balance and agility training, flexibility exercises, and cool-down activities. Exercise intensity will be monitored using the Borg Rating of Perceived Exertion scale and exercise difficulty will be progressively increased by increasing repetitions, walking duration, walking pace, and task complexity.

Sponsors

Çanakkale Onsekiz Mart University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Intervention model description

Participants are assigned to either a 12-week supervised multicomponent exercise group or a control group. Outcomes are assessed at baseline and after the 12-week intervention period.

Eligibility

Sex/Gender
ALL
Age
60 Years to 81 Years
Healthy volunteers
Yes

Inclusion criteria

* being 60 years of age or older, * being able to walk independently, * not having any serious cardiovascular, neurological, or musculoskeletal disease that would prevent exercise. * do not use medications that may affect autonomic nervous system function

Exclusion criteria

* diagnosed cardiac arrhythmia, * uncontrolled hypertension, * use of medications that may affect autonomic nervous system function, * inability to perform functional performance tests.

Design outcomes

Primary

MeasureTime frameDescription
Change in six-minute walk distanceBaseline and 12 weeksFunctional walking capacity will be assessed using the six-minute walk test. The total distance walked in six minutes will be recorded in meters at baseline and after the 12-week intervention.

Secondary

MeasureTime frameDescription
Change in 30-second chair stand test performanceBaseline and after 12 weeksLower-limb functional strength will be assessed using the 30-second chair stand test at baseline and after the 12-week intervention.
Change in 8-foot Up-and-Go test performancebaseline and after 12 weeksFunctional mobility and agility will be assessed using the 8-Foot Up-and-Go test at baseline and after the 12-week intervention.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jul 15, 2026