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

C

Creighton University

Status

Not yet enrolling

Conditions

Age-associated Muscle Loss
Sarcopenia in Elderly
Sarcopenia

Treatments

Behavioral: Experimental: External Focus
Behavioral: Other: Internal Focus

Study type

Interventional

Funder types

Other

Identifiers

NCT06853275
2005068

Details and patient eligibility

About

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

Enrollment

60 estimated patients

Sex

All

Ages

60 to 95 years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

None (Open label)

60 participants in 2 patient groups

External Focus
Experimental group
Treatment:
Behavioral: Experimental: External Focus
Internal Focus
Other group
Treatment:
Behavioral: Other: Internal Focus

Trial contacts and locations

1

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Central trial contact

Rashelle Hoffman, PT, DPT, PhD

Data sourced from clinicaltrials.gov

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