- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06074575
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
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:
|
|
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:
|
|
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:
|
|
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:
|
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.
Sponsor
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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