Pilot study on the possible effectiveness of a three-day treatment program (The Challenge) in persons with chronic pai
- Conditions
- chronic painchronische pijnchronic pain syndromes
- Registration Number
- NL-OMON41138
- Lead Sponsor
- DC Klinieken Rotterdam
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 40
For persons with chronic pain the inclusion criteria are:
1) Diagnosis of chronic pain,
2) Diagnosis at least for 6 months,
3) Willing and able to participate in the study,
4) Written informed consent.
For partners or informal caregivers the inclusion criteria are:
1) Willing and able to participate in the study,
4) Written informed consent.
For persons with chronic pain the exclusion criteria are:
1) No diagnosis of chronic pain,
2) Diagnosis less than 6 months,
3) Not willing or unable to participate in the study,
4) No written informed consent.
For partners or informal caregivers the exclusion criteria are:
1) Not willing or unable to participate in the study,
4) No written informed consent.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>EQ-5D-5L Quality of Life scores, IPA-32 Impact on Participation and Autonomy<br /><br>scores.</p><br>
- Secondary Outcome Measures
Name Time Method <p>VAS Global pain score, SOPA Survey of Pain Attitudes scores, 4DKL Distress,<br /><br>Anxiety, Depression and Somatisation scores.</p><br>