Efficacy and acceptability of the Internet-based self-help program Lenio for individuals with chronic pain and depressive symptoms: a randomized controlled trial.
- Conditions
- R52F32Pain, not elsewhere classifiedDepressive episode
- Registration Number
- DRKS00026722
- Lead Sponsor
- Deutsche Gesetzliche Unfallversicherung e.V. (DGUV)
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 245
An ability to consent (informed consent), available internet access and a smartphone, sufficient understanding of the German language, willingness to participate in three anonymous online surveys, each lasting approximately 25-30min, willingness to participate in a 8-week training program, willingness to use the program at one's own responsibility, presence of chronic pain and depressive symptoms, presence of a desire for treatment, and willingness to leave an email address and receive emails twice a week. For the latter, instructions for creating a free and anonymous email address are provided.
The presence of lifetime schizophrenic or bipolar symptomatology, alcohol dependence, or acute suicidal tendencies are exclusion criteria.
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary outcome is the numeric rating scale pain impairment (mean value of impairment in daily life, leisure time and work) of the German Pain Questionnaire (German acronym: DSF). The primary analysis refers to the difference values between baseline and post time point.
- Secondary Outcome Measures
Name Time Method