Skip to content

Effect of Technology-assisted Physical Therapy for Patient With High Risk of Sarcopenia

Effect of Technology-assisted Physical Therapy for Patient With High Risk of Sarcopenia

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05687630
Acronym
HRS
Enrollment
100
Registered
2023-01-18
Start date
2023-02-01
Completion date
2023-12-30
Last updated
2023-01-18

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

Conditions

Sarcopenia

Keywords

sarcopenia

Brief summary

This research aims to identify whether the effects of video-assisted physical therapy, including home resistance training, is superior to traditional physical therapy, education leaflet for example. This is an interventional research, single-blind, randomized control trail. We recruit high risk of sarcopenia people (low muscle strength and low physical performance) Two groups of participants are divided into traditional group and video-assisted group, both group are taught the same resisted exercise by physical therapist.

Detailed description

Both group will record his/her baseline activity level with a given pedometer. After one week recording, we started initial evaluation (history taking, physical examination) and intervention. Participants are taught thera-band resisted exercise, including large musculature of upper and lower extremities, each exercise are conducted 10-15 times for 3 sets. Traditional group will receive an education leaflet and a notebook to record his/ her daily activity and frequency of exercise to record the compliance. Video-assisted group will receive a QR code, which contain a website of exercise video on the cloud. After 3 months intervention, participant will come back to our center for final examination.

Interventions

OTHERelastic band resisted exercise

muscle strengthening exercise, 10-15 times of each set, for 3 sets

Sponsors

National Taiwan University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
65 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age above 65 years old * MMSE \> 24 points * walking more than 6 meters independently

Exclusion criteria

* people who cannot participate for 3 -day exercise for each week

Design outcomes

Primary

MeasureTime frameDescription
Grip strengththree months after initial evaluationuse hand dynamometer to test maximal strength
walking speedthree months after initial evaluationwalk for 4 meters to test the time that participant used
Timed up-and-go testthree months after initial evaluation

Secondary

MeasureTime frame
Short Physical Performance Battery (SPPB)three months after initial evaluation

Contacts

Primary ContactChen Yu Kuo, Bachelor
119271@ntuh.gov.tw+886 988581069

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026