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Effects of Acute Pain vs Context Change on Motor Learning Retention in Young Adults

Not Applicable
Completed
Conditions
Pain, Acute
Motor Activity
Interventions
Procedure: pain delivery - learning and retention
Procedure: pain delivery - learning only
Registration Number
NCT05626582
Lead Sponsor
University of Delaware
Brief Summary

To date, the effects of pain on motor learning have not been thoroughly investigated. When examining potential effects on retention of motor learning, it is important to dissociate any effects of pain from effects of a context change. The purpose of this research is to determine whether any altered retention of motor learning associated with acute pain is a true affect of pain or an affect of context (or both).

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
61
Inclusion Criteria
  • 18-35 years old
  • Self-identifying as generally medically healthy
  • Able to read, write and speak English
  • Able to provide informed consent
  • Willing to undergo the experimental pain or non-painful electrical stimulation, if selected
Exclusion Criteria
  • Resting HR < 50 or > 100 bpm
  • Resting BP < 90/60 or > 140/95 mmHg
  • Any history or current mental health condition, learning/developmental disability or cognitive impairment, including ADD/ADHD, severe anxiety, severe depression, autism spectrum disorder, insomnia, mild cognitive impairment, etc.
  • Score on the MoCA <23
  • Score on the GAD-7 ≥ 10
  • Score on the PHQ-2 ≥ 2 and score on the PHQ-9 ≥ 10
  • Any current (within last 3 month) or chronic medical conditions, including any musculoskeletal, cardiovascular, endocrine, pulmonary, metabolic, psychiatric or neurological diagnosis
  • Any implanted electronic medical devices (i.e., cardiac pacemakers, cardiac defibrillators, spinal cord neurostimulators)
  • Any impaired sensation or weakness in either lower extremity or in the area targeted for the stimulus
  • 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
  • Taking 4 or more medications
  • 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 permitted, etc.)
  • Any current or chronic pain condition during the last year, located anywhere in the body
  • Allergy to capsaicin or hot peppers
  • Any skin lesion, breakage or irritation in the area targeted for the painful stimulus
  • Skin sensitivity to soaps/creams/perfumes or to heat
  • Poor circulation in the area targeted for the painful stimulus
  • Prior participation in a locomotor learning study in this lab within the last 2 years

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Pain Stimulus - Learning and Retentionpain delivery - learning and retentionCapsaicin combined with heat applied to intact skin
Pain Stimulus - Learning Onlypain delivery - learning onlyCapsaicin combined with heat applied to intact skin
Primary Outcome Measures
NameTimeMethod
Motor Retention Magnitude24 hours post learning (day 2)

degree to which the learned locomotor pattern has been remembered (in step length percent change, normalized to the amount learned from day 1)

Motor Learning Magnitudeimmediately after learning (day 1)

degree to which the new locomotor pattern has been acquired (in step length percent change)

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

University of Delaware

🇺🇸

Newark, Delaware, United States

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