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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05209685
Other study ID # A-BR-110-075
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date August 17, 2020
Est. completion date December 31, 2022

Study information

Verified date November 2023
Source National Cheng Kung University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study investigates the effect of blood flow restriction with resistance exercise on functional mobility in pre-frail older adults. It is hypothesized that receiving resistance exercise with blood flow restriction will exhibit better improvement on functional mobility than only receiving resistance exercise in pre-frail older adults.


Description:

Participants aged over 65 years old with less than two items positive of Fried frailty phenotype assessment result will be recruited. The participants will be randomly assigned to two training groups, blood flow restriction resistance exercise and traditional resistance exercise. Both groups will receive the training 30 minutes/session, two sessions/week for six weeks. Muscle strength of the lower extremities and functional mobility tests will be used to assess outcomes at pre-training, 3-week after training, post-training, and one-month and two-month follow-up.


Recruitment information / eligibility

Status Completed
Enrollment 54
Est. completion date December 31, 2022
Est. primary completion date October 31, 2022
Accepts healthy volunteers No
Gender All
Age group 65 Years to 95 Years
Eligibility Inclusion Criteria: - Aged over 65 years old - Fried frailty index fulfill 1-2 criteria - Able to walk 6 meters independently - Able to understand and follow = 3 instructions Exclusion Criteria: - Severe hypertension (>180/110mmHg) - Peripheral neuropathy - History of deep-vein thrombosis (DVT) - Cardiovascular diseases (i.e. Heart failure NYHA Classification III or IV, myocardial infarction, pulmonary hypertension, coronary artery stenosis) - Neuromuscular diseases (i.e. Stroke, Parkinsons' disease) - History of resisted exercise training program within the last 6 months before screening

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Resistance exercise on the lower extremities
Resistance exercise mainly on the lower extremities will be executed by carrying weight according to each participant's tolerance while performing certain movements, such as side step-up, sit-to-stand, and tip-toe-standing.
Resistance exercise on the lower extremities with blood flow restriction
Blood flow restriction on the thigh of the dominant leg will be used in combination with resistance exercise.

Locations

Country Name City State
Taiwan Department of Physical Therapy Tainan

Sponsors (1)

Lead Sponsor Collaborator
National Cheng Kung University

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change of Timed-Up and Go (TUG) test Timed-Up and Go test Before intervention, 3 and 6 weeks after intervention, and one- and two-month follow ups after intervention
Primary Change of 30 seconds sit to stand 30 seconds sit to stand test Before intervention, 3 and 6 weeks after intervention, and one- and two-month follow ups after intervention
Primary Change of muscle strength of the lower extremities Muscle strength of bilateral hip flexors, knee extensors, ankle dorsiflexors and plantarflexors Before intervention, 3 and 6 weeks after intervention, and one- and two-month follow ups after intervention
Secondary Change of one-repetition maximum One-repetiton maximum of side step-ups Before intervention, 3 and 6 weeks after intervention, and one- and two-month follow ups after intervention
Secondary Change of muscle mass Muscle mass of the upper and lower extremities and trunk Before intervention, 3 and 6 weeks after intervention, and one- and two-month follow ups after intervention
Secondary Change of hand grip strength Bilateral grip strength Before intervention, 3 and 6 weeks after intervention, and one- and two-month follow ups after intervention
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