The Influence of Movement Velocity Biofeedback on Muscle Activation and Self Perception in Older Adults With Sarcopenia (NCT06853275)
🩺 Plain-English Summary (8th-Grade Level)
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
Who can join: To join this study, participants generally need to meet the listed inclusion criteria (4 items) and avoid the listed exclusions (4 items).
Location: Creighton University — Omaha, Nebraska
Age range: 60 Years to 95 Years
🧪 Interventions in This Study
- Experimental: External Focus (BEHAVIORAL)
- Other: Internal Focus (BEHAVIORAL)
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistCheck every box below. If you can check all of them, you may meet the study's basic screening requirements (final eligibility is confirmed by the site team).
Usually NOT eligible if any of the following apply:
- Exclusion Criteria:
- Participated in a structured resistance training program in the last 12 months
- Had a lower extremity injury or surgical intervention within the past 6 months
- Have neuromuscular (i.e., Parkinson's Disease, Multiple Sclerosis), circulatory, or edema pathology
🔍 Extracted verbatim from the official NIH eligibility criteria. Always confirm with the study coordinator.
📍 All Participating Trial Locations (1 Sites)
- Creighton University — Omaha, Nebraska
📞 Contact the Study Coordinator
Phone: (402) 280-5691
Email: rashellehoffman@creighton.edu
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
💰 Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
More studies in Sarcopenia
- The Foods & Oil to Repair, Correct and Enhance Strength (FORCES) Study — Columbus, Ohio
- BandPass: A Remote Monitoring System for Sarcopenia and Functional Decline Phase II Aim 4 — Chapel Hill, North Carolina
- Impacts of Nicotinamide Riboside on Functional Capacity and Muscle Physiology in Older Veterans — Kansas City, Missouri
- Muscle Impact of Treating Osteoporosis — Pittsburgh, Pennsylvania
- Creatine Supplementation During GLP-1a Therapy — Saskatoon, SK - Saskatchewan
Explore by condition: All Sarcopenia clinical trials
💡 How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.