Movement Velocity Biofeedback for Sarcopenia
Trial Summary
Do I need to stop my current medications for the trial?
The trial information does not specify whether you need to stop taking your current medications. It is best to discuss this with the trial coordinators or your doctor.
What data supports the effectiveness of the treatment External Focus, Internal Focus for sarcopenia?
How does the treatment 'External Focus' differ from other treatments for sarcopenia?
The 'External Focus' treatment, involving movement velocity biofeedback, is unique because it emphasizes using feedback to improve movement speed, which is not a common focus in traditional sarcopenia treatments like resistance training or protein supplementation. This approach may help enhance muscle function by encouraging faster and more efficient movements, potentially offering a novel way to address muscle decline in older adults.36789
What is the purpose of this trial?
The overall objective for this clinical trial is to provide evidence for internal and external cueing for physical therapists and other rehabilitation clinicians to optimize resistance training within rehabilitation for older adults. The main questions it aims to answer are:* What is the impact of external focus (providing velocity of movement for each repetition) compared to internal focus (i.e., no cues, control group) on physical percent velocity loss and neuromuscular activation in older adults with sarcopenia?* Does internal and external focus influence motivation and perceptual workload following resistance training in older adults with sarcopenia?Researchers will compare external focus to internal focus to see if external focus impacts percent velocity loss, motivation, and perceived workload.Participants will:* Visit the lab once per week for 3 weeks* Perform exercise testing using a leg press* Answer questionnaires regarding perceived workload and motivation before and after exercise
Eligibility Criteria
This trial is for older adults with sarcopenia, which is a condition involving muscle loss. Participants should be able to visit the lab weekly for three weeks and perform leg press exercises. Specific inclusion or exclusion criteria are not provided.Inclusion Criteria
Exclusion Criteria
Timeline
Screening
Participants are screened for eligibility to participate in the trial
Treatment
Participants perform exercise testing using a leg press and answer questionnaires regarding perceived workload and motivation
Follow-up
Participants are monitored for safety and effectiveness after treatment
Treatment Details
Interventions
- External Focus
- Internal Focus
Find a Clinic Near You
Who Is Running the Clinical Trial?
Creighton University
Lead Sponsor
Foundation for Physical Therapy Research
Collaborator