Lifestyle Modification Program for Patients With Chronic Pain Conditions
CompletedNCT01805947
View the official record on ClinicalTrials.gov Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.
This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.
Brief summary (from the registry)
In this observational study the effects of a Lifestyle Modification Program - offered as a semi-residential day care clinic - on pain, disability, quality of life and satisfaction with life will be investigated. Furthermore the influence of mindfulness, acceptance and coping, and acquired changes in lifestyle behaviors on the outcome after the program will be evaluated. Effects will be measured after completion of the program (3 months), and at 6 and 12 months follow up after start of the program, i.e. each outcome measure will be taken 4 times within 12 months.
Study details
- Official title
- Process-outcome-study in the Context of a Lifestyle Modification Program for Patients With Chronic Pain Conditions
- Conditions
- Interventions
- Behavioral: Lifestyle Modification
- Sponsor
- Universität Duisburg-Essen
- Collaborators
- University of Witten/Herdecke
- Start date
- 2013-01
- Primary completion
- 2015-04
- Sex
- All
- Age range
- from 18 Years to 75 Years
- Results posted
- No results posted in this snapshot
- Countries
- Germany
- Total sites listed
- 1
Eligibility criteria
Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * 18-78 * diagnosed with any chronic pain condition * physical and mental ability to participate in the program and the study * written informed consent Exclusion Criteria: * participation in any other clinical study focusing on psychological or behavioral intervention
Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT01805947