NCT06840743

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.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
180

participants targeted

Target at P75+ for not_applicable

Timeline
Completed

Started Aug 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

February 12, 2025

Completed
9 days until next milestone

First Posted

Study publicly available on registry

February 21, 2025

Completed
6 months until next milestone

Study Start

First participant enrolled

August 31, 2025

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 30, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 30, 2025

Completed
Last Updated

December 30, 2025

Status Verified

February 1, 2025

Enrollment Period

2 months

First QC Date

February 12, 2025

Last Update Submit

December 27, 2025

Conditions

Keywords

Pressure Pain ThresholdsPainEmotions

Outcome Measures

Primary Outcomes (1)

  • Pressure pain thresholds (PPTs)

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

    For each participant, baseline PPTs are measured, intervention follows and intervention PPTs are measured. This will be conducted at one appointment (30 min) for each participant. Recruitment for single appointments will take place for 18 months.

Secondary Outcomes (3)

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

    At 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. Participants are successively recruited for single appointmentsfor 18 months.

  • Pain intensity on the NRS

    The pain intensity will be estimated at every single session appointment (30 min) after the intervention on the NRS (Numerical Rating Scale). The participants will be successively recruited for single session appointments for 18 months.

  • Pain-related negative affect on the NRS-A

    Negative affect will be estimated at every single test session (30 min) on the NRS-A (Numerical Rating Scale-Anxiety) directly after the intervention. The participants will be successively recruited for single session appointments during 18 months.

Study Arms (1)

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

EXPERIMENTAL

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

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

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

Eligibility Criteria

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

You may qualify if:

  • Above 18 years of age
  • Fluent in Swedish.

You may not qualify if:

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Linnaeus University

Vaxjo, 343 32, Sweden

Location

MeSH Terms

Conditions

Pain

Condition Hierarchy (Ancestors)

Neurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
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 12, 2025

First Posted

February 21, 2025

Study Start

August 31, 2025

Primary Completion

October 30, 2025

Study Completion

October 30, 2025

Last Updated

December 30, 2025

Record last verified: 2025-02

Locations