Skip to content

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

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

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05626582
Enrollment
61
Registered
2022-11-23
Start date
2023-04-11
Completion date
2024-05-31
Last updated
2024-07-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Motor Activity, Pain, Acute

Keywords

acute pain, young adults, pain, motor learning, motor consolidation, gait, locomotion, walking, generalization

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).

Interventions

PROCEDUREpain delivery - learning only

Experimental pain paradigm delivered (capsaicin cream combined with heat) that is short-term and painful but not harmful. Applied to skin just during the Day 1 learning period.

PROCEDUREpain delivery - learning and retention

Experimental pain paradigm delivered (capsaicin cream combined with heat) that is short-term and painful but not harmful. Applied to skin during the Day 1 learning period and again during the Day 2 retention period.

Sponsors

National Institute on Aging (NIA)
CollaboratorNIH
University of Delaware
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
NONE

Masking description

Application of pain or no stimulus cannot be masked from participants, nor from outcomes assessors.

Eligibility

Sex/Gender
ALL
Age
18 Years to 35 Years
Healthy volunteers
Yes

Inclusion criteria

Abbreviations: HR= heart rate, bpm= beats per minute; BP= blood pressure; ADD= attention deficit disorder; ADHD= attention deficit hyperactivity disorder; MoCA= Montreal Cognitive Assessment; GAD-7= Generalized Anxiety Disorder 7 Scale; PHQ-2, PHQ-9= Patient Health Questionnaire-2 and -9. 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

Design outcomes

Primary

MeasureTime frameDescription
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)

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026