Clinical trial Recruiting at 1 site Interventional Ages 60 to 95

Movement-speed biofeedback to improve muscle activation and self-perception in older adults with sarcopenia

Official title: The Influence of Movement Velocity Biofeedback on Muscle Activation and Self Perception in Older Adults With Sarcopenia

Run by Creighton University · NCT06853275 · Data updated 2026-11-12

This test will see if giving older adults with sarcopenia feedback on how fast they move during leg-press exercises helps preserve movement speed, increase muscle activation, and change motivation and perceived effort.

Quick facts

Study typeInterventional
Ages60 Years to 95 Years
SexAll
Enrollment60 (estimated)
SponsorCreighton University
Academic / other
Locations1 site (Omaha, Nebraska)
StatusRecruiting
StartedAugust 1, 2025
Main results expectedDecember 31, 2027
Study endsDecember 31, 2027
Registry record updatedMarch 18, 2026
Trial IDNCT06853275 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Community-dwelling, physically independent adults aged 60–95 who are cognitively intact, score 4 or higher on the SARC-F, have not done structured resistance training in the past year, and have no recent lower-limb injury or major neuromuscular or circulatory conditions are the intended participants.

Probably not a fit

People with recent lower-extremity injury or surgery, active neuromuscular or circulatory disease, significant edema, severe cognitive impairment, or those already engaged in regular resistance training are unlikely to benefit or are excluded.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

Older adults with sarcopenia will be assigned to either an external-focus group that receives real-time movement-velocity feedback or to an internal-focus control group with no cues. Participants visit the lab once per week for three weeks to perform leg-press exercise testing while researchers measure percent velocity loss and neuromuscular activation and collect questionnaires on motivation and perceived workload. Exclusion criteria include recent structured resistance training, recent lower-extremity injury or surgery, and neurologic or circulatory conditions that affect movement. The trial tests whether external velocity biofeedback changes short-term performance metrics and participants' perceived workload and motivation.

Why it matters

Potential benefit: If successful, velocity biofeedback could help therapists tailor resistance training to better maintain muscle power and motivation in older adults with sarcopenia.

How similar studies have gone: Related work on velocity-based training and movement biofeedback has shown improvements in power and motor performance in younger and general older populations, but direct evidence in sarcopenic older adults is limited, making this a relatively novel application.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Community-dwelling older adults 60-95 years of age
* Physically independent
* Free of severe mental impairment
* Score 4 or greater on the SARC-F sarcopenia questionnaire

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

Where it's running

  • Creighton University
    Omaha, Nebraska, United States
    Recruiting

Study contacts

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.