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Pilot study for the evaluation of the feasibility and the efficacy of a combined cognitive-behavioral and physiotherapeutic treatment program for patients with Chronic Pelvic Pain Syndrome (CPPS) within the context of the Interdisciplinary Research Platform „Chronic Pelvic Pain Syndrome (CPPS)

Phase 2
Conditions
CPPS (Chronic Pelvic Pain Syndrome)
F45.4
Persistent somatoform pain disorder
Registration Number
DRKS00009976
Lead Sponsor
Institut und Poliklinik für Psychosomatische Medizin und Psychotherapie, Universitätsklinikum Hamburg-Eppendorf
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
54
Inclusion Criteria

Daignosis of CPPS without explaining medical condition, sufficient knowledge of the German language, a score = 40 either in the physical or the mental scale of the SF-12 (health-related quality of life)

Exclusion Criteria

Substance dependence; delusional disorder

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Health-related quality of life (SF-12); 7 times of measurement: at the time of visiting the outpatient clinic, at the time of inclusion, before and after each treatment module as well as four weeks after the overall treatment
Secondary Outcome Measures
NameTimeMethod
Symptom severity (NIH-CPSI), pain perception (SF-MPQ), pain-related disability (PDI), catastrophizing cognitions (PCS), psychological symptom severity (PHQ-9, PHQ-15, GAD-7, PSQ) and utilization of the health care system provided as paper-and-pencil questionnaires; 7 times of measurement: at the time of visiting the outpatient clinic, at the time of inclusion, before and after each treatment module as well as four weeks after the overall treatment (PDI not measured at time of visiting the outpatient clinic); goal attainment (GAS): after the physiotherapeutic module and four weeks after overall treatment; satisfaction with the treatment: before the second module as well as four weeks after the overall treatment; additionally physiotherapeutic examination before the first and before the second treatment module as well as four weeks after the overall treatment
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