Impact of Social Support and Coping Strategies on Post-Surgical Pain

NCT ID: NCT05009316

Last Updated: 2024-04-10

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

368 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-09-20

Study Completion Date

2024-03-21

Brief Summary

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The purpose of the study is to evaluate the impact of social support and pain coping strategies in the development and evolution of post-surgical pain.

Detailed Description

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This is a longitudinal study. After giving their informed consent, patients will answer online questionnaires assessing pain and different psychosocial variables at these time points: before surgery, one to three days after surgery, and one, three, and six months after surgery.

The psychosocial variables evaluated are the following ones :

* Depression,
* Anxiety,
* Stress,
* Pain Coping Strategies,
* Social Support,
* Couple Support.

Conditions

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Social Support Coping Behavior Post-Surgical Pain, Chronic

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

PREVENTION

Blinding Strategy

NONE

Study Groups

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Questionnaires

Patients will answer online surveys containing different questionnaires that will evaluate psychosocial variables as well as pain variables.

Group Type EXPERIMENTAL

Questionnaires

Intervention Type OTHER

Online-based questionnaires

Interventions

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Questionnaires

Online-based questionnaires

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Aged over 18 years of age.
* Capacity to understand and voluntarily sign an informed consent form in French.

Exclusion Criteria

* Insufficient French language skills.
* History of psychotic disease.
* History of neurodegenerative pathology.
* History of neurological disease (e.g. stroke)
* Pre-existing pain condition related to the reason for surgery
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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European Commission

OTHER

Sponsor Role collaborator

Université Catholique de Louvain

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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André Mouraux, Ph.D

Role: STUDY_CHAIR

Université Catholique de Louvain

Locations

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Institute of NeuroScience (IONS) - UCLouvain

Brussels, , Belgium

Site Status

Countries

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Belgium

Other Identifiers

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POPQUEST

Identifier Type: -

Identifier Source: org_study_id

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