Skip to content

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)“

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)“ - COMBI-CPPS

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
DRKS
Registry ID
DRKS00009976
Enrollment
54
Registered
2016-03-15
Start date
2016-06-07
Completion date
Unknown
Last updated
2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

CPPS (Chronic Pelvic Pain Syndrome) F45.4

Interventions

Group 1: Cognitive-behavioral therapy followed by physiotherapy. The manual for the psychotherapeutic intervention was created by our workgroup and is based on the preliminary works of a Canadian wor
the manual treatment of myofascial trigger points
methods to influence the diaphragmatic activity
instruction of the participants in self-treatment and supervision of the self-exercises. Between the interventions, there will be a four-week pause. Group 2: Physiotherapy followed by cognitive-beha
for a description of the modules see "Arm 1" Group 3: Control group -

Sponsors

Institut und Poliklinik für Psychosomatische Medizin und Psychotherapie, Universitätsklinikum Hamburg-Eppendorf
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

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

Exclusion criteria: Substance dependence; delusional disorder

Design outcomes

Primary

MeasureTime frame
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

MeasureTime frame
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

Countries

Germany

Contacts

Public ContactChristoph Dybowski

Institut und Poliklinik für Psychosomatische Medizin und Psychotherapie, Universitätsklinikum Hamburg-Eppendorf

c.dybowski@uke.de+49 (0) 7410 - 52997

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Mar 7, 2026