NCT06851208

Brief Summary

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.

Trial Health

65
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
180

participants targeted

Target at P75+ for not_applicable

Timeline
2mo left

Started Mar 2026

Shorter than P25 for not_applicable

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Progress56%
Mar 2026Jun 2026

First Submitted

Initial submission to the registry

February 21, 2025

Completed
7 days until next milestone

First Posted

Study publicly available on registry

February 28, 2025

Completed
1 year until next milestone

Study Start

First participant enrolled

March 1, 2026

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

June 30, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

June 30, 2026

Last Updated

February 28, 2025

Status Verified

February 1, 2025

Enrollment Period

4 months

First QC Date

February 21, 2025

Last Update Submit

February 26, 2025

Conditions

Keywords

Pressure pain thresholdsPainEmotions

Outcome Measures

Primary Outcomes (1)

  • Pressure pain thresholds

    Description: Pressure pain thresholds will be measured i kPa with a handheld algometer (Somedic AB).

    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 Outcomes (3)

  • Pain tolerance (time in seconds the left hand is immersed in cold water 1 degree C).

    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

    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

    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.

Study Arms (1)

Experimental: Negative emotion, positive emotion, neutral emotion, control with experimental pain

EXPERIMENTAL

Arm Description: The intervention includes either a negatively emotionally valenced video, a positively emotionally valenced video, a neutrally emotionally valenced video and experimental pain from the cold pressor test that are simultaneosly applied.

Other: Emotional intervention

Interventions

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

Experimental: Negative emotion, positive emotion, neutral emotion, control with experimental pain

Eligibility Criteria

Age19 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

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

You may not qualify if:

  • \- Known neurological disease

Contact the study team to confirm eligibility.

Sponsors & Collaborators

MeSH Terms

Conditions

Pain

Condition Hierarchy (Ancestors)

Neurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Central Study Contacts

Helena Gunnarsson, Dr

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
BASIC SCIENCE
Intervention Model
PARALLEL
Model Details: Within-subjects design
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Dr

Study Record Dates

First Submitted

February 21, 2025

First Posted

February 28, 2025

Study Start

March 1, 2026

Primary Completion (Estimated)

June 30, 2026

Study Completion (Estimated)

June 30, 2026

Last Updated

February 28, 2025

Record last verified: 2025-02