Effects of a depression-focused internet intervention in patients with acute pain: A randomized controlled trial
Phase 2
- Conditions
- F32R52Depressive episodePain, not elsewhere classified
- Registration Number
- DRKS00015222
- Lead Sponsor
- IVP-Networks GmbH, Psychiatrische Versorgung in Hamburg
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 157
Inclusion Criteria
•age: 18 to 75 years old
•consent to participate in study (informed consent)
•internet access
•sufficient understanding of the German language
•willingness to participate in two anonymous online surveys, each of which lasts approx. 25-30 minutes
•willingness to participate in an 12-week training program
•willingness to use the program on one's own responsibility
•willingness to provide an e-mail address
•presence of current or reported depressive symptoms
•acute pain (with a focus on back pain, 1/3 participants with back pain are planned to be recruited)
Exclusion Criteria
•lifetime schizophrenic or bipolar symptoms
•acute suicidal tendencies
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Beck Depression Inventar-II (BDI-II): A self-rating questionnaire to measure depressive symptoms over the past two weeks
- Secondary Outcome Measures
Name Time Method