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Clinical Trials/NCT04057664
NCT04057664
Terminated
N/A

Managing the Pain - a Group Therapy Based on the Bio-psycho-social Treatment Approach for Women With Chronic Pelvic Pain and Chronic Belly Pain

Swiss Paraplegic Research, Nottwil1 site in 1 country8 target enrollmentSeptember 1, 2020

Overview

Phase
N/A
Intervention
Learning of Coping Strategies
Conditions
Pain, Chronic
Sponsor
Swiss Paraplegic Research, Nottwil
Enrollment
8
Locations
1
Primary Endpoint
Change in Pelvic Pain Impact Questionnaire (PPIQ)
Status
Terminated
Last Updated
2 months ago

Overview

Brief Summary

The project investigates the situation of patients with chronic pelvic and chronic belly pain before and after our group therapy.

Detailed Description

To treat patients with chronic pelvic and belly pain in an interdisciplinary way, we developped a group therapy consisting of twelve sessions and a booster session. The therapy is based on the bio-psycho-social model of pain and includes group sessions of psychotherapy as well as physiotherapy. All patients fill in questionnaires (concerning pain impact, pain chronicity, depression, anxiety, stress, well-being and sexuality) before and after the therapy as well as three and twelve months after.

Registry
clinicaltrials.gov
Start Date
September 1, 2020
End Date
December 4, 2024
Last Updated
2 months ago
Study Type
Observational
Sex
Female

Investigators

Sponsor
Swiss Paraplegic Research, Nottwil
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Women with chronic pelvic pain or belly pain participating in our group therapy who give their consent to the analysis of their data for the study

Exclusion Criteria

  • No participation in the group therapy
  • Finishing the group therapy prematurely (\>3 missed sessions)

Arms & Interventions

Multidisciplinary Group Therapy

Multidisciplinary group therapy for women with chronic pelvic or belly pain

Intervention: Learning of Coping Strategies

Outcomes

Primary Outcomes

Change in Pelvic Pain Impact Questionnaire (PPIQ)

Time Frame: baseline, 6 weeks, 3 months, 12 months

Self reported questionnaire with 8 questions to assess the impact of pelvic pain on quality of life, daily activities and emotional life. Each questions is scored 0-4, yielding a total from 0 and 32.

Secondary Outcomes

  • Change in Female Sexual Distress Scale-Revised (FSDS-R)(baseline, 6 weeks, 3 months, 12 months)
  • Change in Anxiety(baseline, 6 weeks, 3 months, 12 months)
  • Change in Stress(baseline, 6 weeks, 3 months, 12 months)
  • Change in Sexual Functioning Questionnaire (CSFQ-14)(baseline, 6 weeks, 3 months, 12 months)
  • Change in Chronic Pain Grade Scale (CPGS)(baseline, 6 weeks, 3 months, 12 months)
  • Change in Depression(baseline, 6 weeks, 3 months, 12 months)

Study Sites (1)

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