NCT05687630

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.

Trial Health

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
100

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Feb 2023

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

January 8, 2023

Completed
10 days until next milestone

First Posted

Study publicly available on registry

January 18, 2023

Completed
14 days until next milestone

Study Start

First participant enrolled

February 1, 2023

Completed
10 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 30, 2023

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

December 30, 2023

Completed
Last Updated

January 18, 2023

Status Verified

August 1, 2022

Enrollment Period

10 months

First QC Date

January 8, 2023

Last Update Submit

January 8, 2023

Conditions

Sarcopenia

Keywords

sarcopenia

Outcome Measures

Primary Outcomes (3)

  • Grip strength

    use hand dynamometer to test maximal strength

    three months after initial evaluation

  • walking speed

    walk for 4 meters to test the time that participant used

    three months after initial evaluation

  • Timed up-and-go test

    three months after initial evaluation

Secondary Outcomes (1)

  • Short Physical Performance Battery (SPPB)

    three months after initial evaluation

Study Arms (2)

Video-assisted group

EXPERIMENTAL
Other: elastic band resisted exercise

Traditional group

ACTIVE COMPARATOR
Other: elastic band resisted exercise

Interventions

elastic band resisted exerciseOTHER

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

Also known as: resisted exercise
Traditional groupVideo-assisted group

Eligibility Criteria

Age65 Years+
Sexall
Healthy VolunteersNo
Age GroupsOlder Adult (65+)

You may qualify if:

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

You may not qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Sarcopenia

Condition Hierarchy (Ancestors)

Muscular AtrophyNeuromuscular ManifestationsNeurologic ManifestationsNervous System DiseasesAtrophyPathological Conditions, AnatomicalPathological Conditions, Signs and SymptomsSigns and Symptoms

Study Officials

  • Chen Yu Kuo, Bachelor

    National Taiwan University Hospital

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Chen Yu Kuo, Bachelor

CONTACT

+886 988581069119271@ntuh.gov.tw

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
PARTICIPANT
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

January 8, 2023

First Posted

January 18, 2023

Study Start

February 1, 2023

Primary Completion

November 30, 2023

Study Completion

December 30, 2023

Last Updated

January 18, 2023

Record last verified: 2022-08

Data Sharing

IPD Sharing
Will not share