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Clinical Trials in Sweden / NCT05147948
Recruiting Not applicable

iACT for PTSD and Chronic Pain

NCT05147948 · tracked via the Priya Life Science Sweden tracker
Sponsor
Skane University Hospital
Phase
Not applicable
Started
2021-10-18
Last updated
2026-02-19

Condition(s) studied

PtsdChronic Pain

Investigational drug(s) / intervention(s)

iACT for PTSD and Chronic Pain

iACT for PTSD and Chronic Pain: The participants will go through internet-based Acceptance and Commitment Therapy which mainly involves: 1) Exercises focused on developing acceptance, defusion, and mindfulness skills; 2) Identification of personal values as well as valued steps and feared situations to approach during the program 3) Written exposure exercises focusing on the traumatic memory adapted from Written exposure therapy (WET) using an ACT-based framework. The treatment is delivered on a safe internet platform. Participants have planned telephone contact with their assigned psychologist 3 times during the program and can also contact their psychologist via a message system in the platform and expect answer within 48 hours.

Study summary

The primary aim of this study is to investigate the effect of Internet-delivered Acceptance and commitment therapy for PTSD and comorbid chronic pain using a randomized controlled trial with waitlist control.

Eligibility

Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
No
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))

Primary outcome measure(s)

  • PTSD symptom severity as measured by the the Posttraumatic Stress Disorder Checklist for DSM-5 (PCL-5) and the Life Events Checklist (LEC-5) — Baseline, mid-treatment (3 weeks), mid-treatment (7 weeks), two-week-post treatment, 3 month-follow-up, 12-month follow-up.
    (changes between assessments)

Trial sites (1)

FacilityCityRegionStatus
Department of Pain Pehabilitation, Skåne University Hospital Lund Sweden Recruiting

More Skane University Hospital trials in Sweden

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The Swedish BioFINDER - Memory Clinic Study Recruiting
Internet-based ACT for Endometriosis and Chronic Pain Recruiting
Selenium Intervention Registry Randomized Trial in Heart Failure Recruiting

Other trials for the same condition

Internet-Delivered ACT Targeting Emotional Distress and Chronic Pain Recruiting
Pain Reprocessing Therapy (PRT) in a Specialist Pain Clinic: A Feasibility Study Recruiting
Development of a Pain Rehabilitation Program for Chronic Pain After SCI Starting soon
Trauma-adapted Yoga in Child & Adolescent Psychiatry. Recruiting
Internet-based ACT for Endometriosis and Chronic Pain Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05147948 on ClinicalTrials.gov ↗ ← All trials in Sweden