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Not yet recruiting NCT06851208

Do Emotions and Pain Combined Affect Mechanical Pain Thresholds and Other Pain-related Variables in Individuals with Chronic Pain?

No phase Interventional Pain Thresholds Pain Intensity

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Emotional intervention, Emotional intervention, Emotional intervention.
Who it may be relevant to
Registry conditions: Pain Thresholds, Pain Intensity. Basic parameters: from 19 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Center list to be confirmed — check the primary protocol.
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

The purpose of this study is to investigate if different emotional states could influence mechanical pain thresholds and other pain - related variables such as pain tolerance, pain intensity and pain - related negative affect in individuals with chronic pain.

Detailed description

Participants with chronic pain will be randomized into 4 different groups watching different short video-clips (2.20 min), while at the same time experience short-lasting, experimentally induced pain. The negative emotions group will watch an uncomfortable short video containing violence and blood, the positive emotions group will watch a video containing a stand-up comedy show, the neutral emotions group will watch a video about how to paint a house, and the control group will just wait for 2.20 min, without any instructions about what to think about. Pressure pain thresholds, pain tolerance, pain intensity and pain-related negative affect will be measured with an algometer before and after the video-clip combined with experimental pain interventions.

Interventions

  • Other Emotional intervention
    Emotional intervention Description: The participant will watch a short video-clip with negative emotional content while simultaneously experience experimentally induced pain.
  • Other Emotional intervention
    Description: The participant will watch a short video-clip with positive emotional content while simultaneously experience experimentally induced pain.
  • Other Emotional intervention
    Description: The participant will watch a short video-clip with neutral emotional content while simultaneously experience experimentally induced pain.

Primary outcome measures

  • Pressure pain thresholds [Time frame: Day 1: baseline PPTs are measured, intervention 2.20 min follows and intervention PPTs are measured directly after the intervention. Recruitment for single appointments for each participant will take place for 4 months.]
Secondary outcome measures (3)
  • Pain tolerance (time in seconds the left hand is immersed in cold water 1 degree C). [Time frame: Day 1: During a single session (30 min), the participant will keep their hand immersed in cold water for as long as possible while watching a video. This time will be measured in seconds.]
  • Pain intensity on the NRS [Time frame: Day 1: Pain intensity will be estimated at single session appointments (30 min) on the NRS (Numerical Rating Scale) after the intervention. Participants will be successively recruited for single session appointments for 4 months.]
  • Pain-related negative affect on the NRS-A [Time frame: Day 1: Pain intensity will be estimated at single session appointments (30 min) on the NRS-A (Numerical Rating Scale-Anxiety) after the intervention. Participants will be successively recruited for single session appointments for 4 months.]

Eligibility criteria

Inclusion criteria

  • Above 18 years of age
  • Fluent in Swedish
  • Persistent chronic pain with duration > 6 months

Exclusion criteria

\- Known neurological disease

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Basic science

Study locations

Center list to be confirmed — check the primary protocol.

Identifiers

NCT: NCT06851208 · 2024-07781-01 ethic approval

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗