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Pilot study on the possible effectiveness of a three-day treatment program (The Challenge) in persons with chronic pai

Completed
Conditions
chronic pain
chronische pijn
chronic 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
Inclusion Criteria

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.

Exclusion Criteria

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
NameTimeMethod
<p>EQ-5D-5L Quality of Life scores, IPA-32 Impact on Participation and Autonomy<br /><br>scores.</p><br>
Secondary Outcome Measures
NameTimeMethod
<p>VAS Global pain score, SOPA Survey of Pain Attitudes scores, 4DKL Distress,<br /><br>Anxiety, Depression and Somatisation scores.</p><br>
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