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

  • STATUS
    Recruiting
  • End date
    Mar 3, 2024
  • participants needed
    500
  • sponsor
    Université Catholique de Louvain
Updated on 24 May 2022

Summary

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.

Description

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.

Details
Condition Social Support, Coping Behavior, Post-Surgical Pain, Chronic
Treatment Questionnaires
Clinical Study IdentifierNCT05009316
SponsorUniversité Catholique de Louvain
Last Modified on24 May 2022

Eligibility

Yes No Not Sure

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
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How to participate?

Step 1 Connect with a study center
What happens next?
  • You can expect the study team to contact you via email or phone in the next few days.
  • Sign up as volunteer to help accelerate the development of new treatments and to get notified about similar trials.

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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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