Viewing Study NCT05697497



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Last Modification Date: 2024-10-26 @ 2:50 PM
Study NCT ID: NCT05697497
Status: COMPLETED
Last Update Posted: 2023-08-18
First Post: 2022-02-08

Brief Title: Functional Activity Strength Training
Sponsor: Milton S Hershey Medical Center
Organization: Milton S Hershey Medical Center

Study Overview

Official Title: A Brief Digital Exercise Program to Improve Physical Function Among Older Adults
Status: COMPLETED
Status Verified Date: 2023-08
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: FAST
Brief Summary: This study is a randomized trial of 100 older adults with mobility disability who performed a similar brief daily resistance training program The investigators set out to answer the following question Will a digital brief daily exercise program be feasible acceptable and effective among older adults with walking limitations To answer that question participants were assigned to an intervention or delayed-treatment control group Intervention participants were assigned to complete two 30-second lower body exercises and two 30-second upper body exercises Fitness tests were completed remotely three times during the 12-weeks ie at baseline week 6 week 12
Detailed Description: This is a 12-week delayed-control randomized trial to answer the following question Will a digital brief daily exercise program be feasible acceptable and effective among older adults with walking limitations Participants who screen eligible will be assigned to one of four conditions an immediate workout group an immediate workout group with activity monitor a delayed workout group or a delayed workout group with activity monitor Participants will complete a daily 25-to-35-minute exercise routine at home and to record their results using an electronic survey Other outcome measurements will be conducted remotely at baseline 6 and 12 weeks

The investigators hypothesize that participants in the AMRAP condition will report significant reductions in functional physical limitations increased gait speed and increased physical performance ie increased exercise repetitions from baseline to 6 weeks compared to those randomized to the delayed-treatment control

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None