Pain and Split-belt Motor Learning in Older Adults

Not Applicable

Not yet recruiting

• Conditions: Aging; Older Adults; Pain; Motor Learning

• Registration Number: NCT07054840
• Lead Sponsor: University of Delaware

Brief Summary

The purpose of this research is to investigate the impact of acute pain, induced using an experimental pain paradigm of capsaicin paired with heat, on implicit locomotor learning and its retention in older adults.

Detailed Description

Not available

Study Timeline

• Study First Submitted: 2025-06-27
• Study First Submitted QC: 2025-06-27
• Status Verified: 2025-07
• Study First Posted: 2025-07-08
• Last Update Submitted: 2025-07-08
• Last Update Posted: 2025-07-11
• Study Start: 2025-08-15
• Primary Completion: 2026-05-31
• Study Completion: 2026-05-31

Recruitment & Eligibility

• Status: NOT_YET_RECRUITING
• Sex: All
• Target Recruitment: 34

Inclusion Criteria

• Age 55-90 years old
• Self-identifying as generally medically healthy
• Able to read, write and speak English
• Able to provide informed consent and attend all testing sessions
• Willing to undergo the experimental pain paradigm, if selected

Exclusion Criteria

• Resting heart rate < 50 or > 100 bpm
• Resting blood pressure < 90/60 or > 165/95
• Any history or current mental health condition, learning/developmental disability or cognitive impairment, including severe untreated ADD/ADHD, severe untreated anxiety, severe untreated depression, autism spectrum disorder, insomnia, mild cognitive impairment, etc. (Mild to moderate treated ADD/ADHD, anxiety, and/or depression are allowed.)
• Score on the Montreal Cognitive Assessment (MoCA) <23
• Score on the Generalized Anxiety Disorder-7 Scale ≥ 10
• Score on the Patient Health Questionnaire-2 ≥ 2 and score on the Patient Health Questionnaire-9 ≥ 10
• Any current (within last 3 month) or chronic medical conditions, including any musculoskeletal, cardiovascular, pulmonary, metabolic, psychiatric or neurological diagnosis that affects activities of daily living or would confound testing or place the subject at risk by participating, such as a significant cardiovascular condition or event (e.g., heart attack < 3 months ago, uncontrolled atrial fibrillation, uncontrolled angina, congestive heart failure, chronic obstructive pulmonary disorder, or peripheral vascular disease)
• Any impaired sensation or weakness in either lower extremity
• History of serious concussion or head injury, defined as a loss of consciousness for > 5 minutes and/or requiring medical treatment, or > 2 concussions over the lifespan
• Any history of acute or chronic problems with balance, any dizziness, or > 1 fall in the last 12 months
• Currently or regularly using any analgesic medications, over-the-counter remedies, or any other treatment for the purposes of pain relief (i.e., baby aspirin for heart health is allowed)
• Any current or chronic pain condition during the last year, located anywhere in the body with an intensity of > 2/10
• Allergy to capsaicin or hot peppers
• Any skin lesion, breakage or irritation in the area targeted for the painful stimulus
• Significant skin sensitivity to soaps/creams/perfumes or to heat
• Poor circulation in the area targeted for the painful stimulus
• Prior participation in a split-belt locomotor learning study in the Neuromotor Behavior Lab in the past 2 years

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Learning magnitude	End of day 1	Step length asymmetry averaged over the last 25 strides of the practice period on day 1.
Retention magnitude	Beginning of day 2.	Step length asymmetry averaged over the first 4 strides of the re-adaptation period on day 2.
Forgetting index	End of day 1 and beginning of day 2.	Difference between retention magnitude and learning magnitude.

Trial Locations

Locations (1)

Health Sciences Complex; 🇺🇸 Newark, Delaware, United States