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Completed

NCT Number: NCT07234123

Cognitive Conditioned Pain Modulation

This "pain reduces pain" study looks at how the brain reduces pain when a person feels two painful sensations at the same time. There is considerable evidence that the brain can "turn down" pain using natural endogenous pain-control systems. The current CPM study measures whether attentional processes can also make a measurable contribution to pain inhibition alongside neurochemical mechanisms.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Washington Seattle

Seattle, Washington, 98195, United States

About this study

Conditioned pain modulation (CPM) is a natural process where feeling pain in one part of the body (e.g., a conditioning stimulus to the wrist) can reduce pain felt in another part of the body (a test stimulus to the foot). There is considerable evidence from both animal and human studies that the painful conditioning stimulus can stimulate the brain to activate neurochemical pain-control pathways (e.g., endogenous opioids), which are believed to take 30-120 seconds to fully engage. The current CPM study measures whether attentional processes can also make a measurable contribution to pain inhibition alongside neurochemical mechanisms.

Primary measures: Graphic ratings scale "worst pain" ratings.

The primary measure of the current study graphic ratings scales (worst pain ratings) will measure how much pain participants feel on their foot during foot only (test stimulus), vs. how much pain participants feel on their foot (test stimulus during simultaneous foot (test stimulus) + wrist (conditioning stimulus).

The current investigators predict that pain (e.g., the conditioning stimulus) naturally demands attention and can pull attention away from the original pain source (the test stimulus), resulting in CPM-like reductions in pain of the test stimulus.

Secondary measure #1. Cognitive measures are introduced in the current study, to quantify how much (if at all) the conditioning stimulus reduces pain of the target stimulus via attentional mechanisms. Participants estimate what percentage of their attention was directed to their foot (the test stimulus) during foot only vs. during foot + wrist (test + conditioning stimulus). This will measure whether the conditiioning stimulus to the wrist reduces how much attention participants focus on their foot. Analyses will also measure whether the amount of attention shift away from the foot (via participants; subjective ratings) is correlated with CPM robustness (reduction in pain of foot during duel stimulation).

Secondary measure #2. As another secondary measure of attention during one vs. two simultaneous pain stimuli, this study involves a divided attention auditory listening task that becomes harder when pain demands more attention (Craik et al., odd number divided attention task during single test pain stimuli vs. simultaneous test + conditioning stimuli). The more errors the participant makes on the divided attention task, the more attention diverted away from the auditory task by pain. Analyses will measure whether the number of errors on the divided attention task is correlated with CPM robustness (reduction in pain of foot, during duel thermal stimulation).

Exploratory measures. As exploratory measures, participants will rate how distracted they were and how difficult it was to concentrate (on 0-10 rating scales during test stimulus alone verses test + conditioning noxious thermal heat stimuli).

In summary, embedding these cognitive measures into the CPM protocol may enhance mechanistic interpretation accuracy by quantifying attentional contributions to pain inhibition in specific CPM protocols, thereby complementing existing approaches to pain phenotyping and reducing unexplained variance in CPM outcomes.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Only University of Washington students in eligible psychological courses are
  • eligible. General public is not eligible.
  • Enrolled psychology students fluent in English,
  • Age ≥18 y, able to follow instructions.

Exclusion criteria

  • Seizure history,
  • Migraines,
  • Diabetes,
  • Extreme pain insensitivity,
  • Motion sickness,
  • or prior participation in this protocol.

Treatment and study plan

conditioned pain modulation

Behavioral

simultaneous stimuli to foot (test stimulus) and wrist (conditioning stimulus)

test stimulus

Behavioral

single brief stimulus to foot only

Primary outcomes

  1. worst pain ratings of foot only

    Time frame: rated immediately after each thermal stimulus

    graphic rating scale from 0 (no pain) to 10 (excruciating pain)

  2. worst pain on graphic rating scale during test+conditioning stimulus

    Time frame: measured immediately after the stimuli

    graphic rating scale from 0 (no pain) to 10 (excruciating pain)

Secondary outcomes

  1. % of attention devoted to foot during test stimulus only (0-100% scale)

    Time frame: rated immediately after the stimuli

    verbal ratings where higher numbers = more attention

  2. % of attention devoted to foot during test+conditioning stimuli (0-100% scale)

    Time frame: rated immediately after the thermal stimuli

    verbal ratings where higher numbers = more attention

  3. Divided attention during test stimulus only (% correct, where 100% is highest accuracy)

    Time frame: Day 1, during the thermal stimulus

    Accuracy monitoring a string of auditory numbers, the odd number task during test stimulus

  4. Divided attention during test stimulus + conditioning stimulus (% correct, 100% is highest )

    Time frame: Day 1, during the thermal stimuli

    Accuracy monitoring a string of auditory numbers, the odd number task during dual stimuli

Other outcomes

  1. distraction difficulty during test stimulus only (0 to 10 scale, where 10 is most distracting)

    Time frame: immediately after the phase 1 thermal stimuli

    Exploratory: Distraction during the single test stimulus (graphic rating scales)

  2. distraction difficult during simultaneous test + conditioning stimuli (graphic rating scale)

    Time frame: Exploratory: immediately after the phase 1 thermal stimuli

    Exploratory: 0-10 distraction during simultaneous test + conditioning stimulus (10 =highest distraction)

  3. difficulty concentrating during test stimulus only (0 to 10 scale, 10 = most difficult concentr

    Time frame: Exploratory: immediately after the phase 1 thermal stimuli

    Exploratory: difficulty concentrating during the single test stimulus (graphic scales)

  4. difficulty concentrating during simultaneous test + conditioning stimuli (graphic rating scale)

    Time frame: Exploratory: immediately after the phase 1 thermal stimuli

    Exploratory: difficulty concentrating during simultaneous test + conditioning stimulus, 10 = most difficult

Sponsors and collaborators

Lead sponsor

University of Washington

Other

Collaborators

  • Mayday Fund

Registry information

Official study title

Conditioned Pain Modulation With Ultra-Brief Conditioning Stimulus

Acronym: CognitiveCPM

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Nov 18, 2025
Registry last updated
Jan 7, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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