Feasibility of At-Home Chair-Based Resistance Band Training to Improve Balance, Strength, and Bone Density in Older Adults

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age50+
SponsorThe University of Texas Health Science Center, Houston

About this trial

The purpose of this study is to determine the feasibility of implementing a 24-week at-home chair-based resistance band training intervention, to determine effectiveness of a the a 24-week at-home chair-based resistance band training intervention in improving body composition and to determine the effectiveness of a 24-week at-home chair-based resistance band training intervention in improving physical performance in adults 50 years and older, receiving care at the UT Physicians Center for Healthy Aging.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

English-speaking

receive care at the UT Physician Center for Healthy Aging

Disqualifiers

inability to provide informed consent on their own

presence of obvious signs of cognitive decline

a diagnosis of dementia and inability to come to the clinic for the scheduled study visits.

Trial design

Design model

Single group

Treatments tested in this trial

  • THERABand resistance exercise bands

    Device

    The training will be performed using THERABand resistance exercise bands.Participants will be instructed to perform the exercises twice per week at home, for the 24 weeks duration. Each exercise session will entail 1 set of 15 repetitions of 9 different exercises

Treatment groups

40 Participants
are divided into 1 treatment group
Group A: Chair-based resistance band trainingExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Feasibility as assessed by the number of people who are able to follow the prescribed exercise regimen at least 50 percent of the time

Time frame
end of study (24 weeks from baseline)

Secondary outcomes

1

Change in body fat

This will be assessed using the handheld bioelectrical impedance analysis (BIA) device (Omron HBF-510)

Time frame
baseline,6-months
2

Change in bone mineral density (BMD) of the femoral neck and lumbar spine

This will be assessed by the Dual energy x-ray absorptiometry (DXA)

Time frame
baseline, 1 year from baseline
3

Handgrip strength

This will be assessed using a validated handgrip dynamometer

Time frame
baseline
4

Handgrip strength

This will be assessed using a validated handgrip dynamometer

Time frame
1-month

Other outcomes

Sponsors and contacts

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This trial is not recruiting at the moment. You can still explore other options: