Do Emotions Affect Mechanical Pain Thresholds? (DEAMPT)

February 12, 2025 updated by: Helena Gunnarsson, Linnaeus University

The Effect of Positive and Negative Emotions on Mechanical Pain Thresholds: a Randomized Controlled Trial

The purpose of this study is to investigate if different emotional states could influence mechanical pain thresholds.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Participants will be randomized into 4 different groups watching different short video-clips (2.20 min). 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 with Swedish nature, and the control group will just wait for 2.20 min, without any instructions about what to think about. Pressure pain thresholds will be measured with an algometer before and after the video-clip interventions.

Study Type

Interventional

Enrollment (Actual)

152

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Kronoberg
      • Växjö, Kronoberg, Sweden, 35195
        • Helena Gunnarsson

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • Above 18 years of age, fluent in Swedish.

Exclusion Criteria:

  • Pain anywhere in body during the test session, known neurological disease.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Basic Science
  • Allocation: Randomized
  • Interventional Model: Sequential Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Negative emotional condition
The participant will watch a short video-clip with negative emotional content.
The participants will receive different emotion inductions through short video clips.
Other Names:
  • Negative emotion induction, positive emotions induction, neutral emotions induction, control.
Experimental: Positive emotional condition.
The participant will watch a short video-clip with positive emotional content.
The participants will receive different emotion inductions through short video clips.
Other Names:
  • Negative emotion induction, positive emotions induction, neutral emotions induction, control.
Experimental: Neutral condition.
The participant will watch a short video-clip with neutral emotional content.
The participants will receive different emotion inductions through short video clips.
Other Names:
  • Negative emotion induction, positive emotions induction, neutral emotions induction, control.
Experimental: Control condition.
The participant will not watch a video-clip, but will wait without specific instructions about what to think about.
The participants will receive different emotion inductions through short video clips.
Other Names:
  • Negative emotion induction, positive emotions induction, neutral emotions induction, control.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Pressure pain threshold
Time Frame: Measurements will be conducted at the test session, which will have a duration of approximately 20 minutes for each participant.
Pressure pain threshold value after each different emotion intervention and control compared to before each emotion intervention and control.
Measurements will be conducted at the test session, which will have a duration of approximately 20 minutes for each participant.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Helena Gunnarsson, PhD, Linnéuniversitetet

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

October 1, 2023

Primary Completion (Actual)

May 10, 2024

Study Completion (Actual)

May 22, 2024

Study Registration Dates

First Submitted

October 3, 2023

First Submitted That Met QC Criteria

October 3, 2023

First Posted (Actual)

October 10, 2023

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

February 12, 2025

Last Verified

October 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • 2023-03968-01

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

YES

IPD Plan Description

Data is available after study completion.

IPD Sharing Time Frame

The data will be available after study completion.

IPD Sharing Access Criteria

The data is anonymous and is therefore freely available.

IPD Sharing Supporting Information Type

  • SAP

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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