Internet-delivered therapy for PTSD and chronic pain
Internet-based Acceptance and Commitment Therapy for PTSD and Chronic Pain
This study is testing whether online therapy can help people with PTSD and chronic pain feel better compared to those who wait to start the treatment.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 40 (estimated) |
| Ages | 18 Years to 65 Years |
| Sex | All |
| Sponsor | Skane University Hospital Academic / other |
| Locations | 1 site (Lund) |
| Trial ID | NCT05147948 on ClinicalTrials.gov |
What this trial studies
This study investigates the effects of Internet-delivered Acceptance and Commitment Therapy (iACT) on individuals suffering from PTSD and chronic pain. It employs a randomized controlled trial design with a waitlist control group, where participants are divided into two groups: one receiving iACT and the other placed on a waitlist for 12 weeks before receiving the same treatment. The study aims to assess the efficacy of this therapeutic approach through baseline and post-treatment evaluations, including self-report measures and clinician-administered assessments. Participants will be recruited from the Pain Rehabilitation Unit at Skåne University Hospital, ensuring a focused approach to chronic pain management.
Who should consider this trial
Good fit: Ideal candidates are individuals with a confirmed diagnosis of PTSD and chronic pain that significantly interferes with daily life.
Not a fit: Patients with severe psychiatric disorders or those who have experienced repeated traumatic events may not benefit from this study.
Why it matters
Potential benefit: If successful, this therapy could significantly improve the quality of life for patients suffering from both PTSD and chronic pain.
How similar studies have performed: Other studies have shown promise with similar Internet-delivered therapeutic approaches for mental health conditions, suggesting potential for success in this area.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * a CAPS of ≥25 * subjected to single traumatic events * were able to understand Swedish * had symptoms of chronic pain that interfered significantly with everyday life * were fully examined medically and had received medical treatment if indicated * were able to be an active part of the rehabilitation process, regain functioning in different life areas and participate in treatment interventions for approximately 5 hours every week * stable dose of medication * able to read and write in Swedish * had access to a smart phone or computer with internet access Exclusion Criteria: * repeated and extensive traumatic events * had other acute or severe psychiatric disorders or symptoms that warranted designation as the primary disorder (ongoing substance dependence, untreated bipolar disorder, OCD, psychotic symptoms, severe depression) * were actively abusing analgesic medications (including narcotics), alcohol or other drugs * had great difficulty to harbour and handle strong emotions that could lead to emotional outbursts or self-harming behavior * had health risks due to medical reasons * had social or economic difficulties or lack of social support that hindered behavior change * current severe suicidal ideation that warranted immediate intervention (indicated by the MINI and a score of 3 to item 9 of the Patient Health Questionnaire 9-item version (PHQ9))
Where this trial is running
Lund
- Department of Pain Pehabilitation, Skåne University Hospital — Lund, Sweden (Recruiting)
Study contacts
- Study coordinator: Sophia Åkerblom, PhD
- Email: Sophia.akerblom@psy.lu.se
- Phone: 0046707790415
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.