Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
NCT05147948

iACT for PTSD and Chronic Pain

Led by Skane University Hospital · Updated on 2026-02-19

40

Participants Needed

1

Research Sites

321 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

iACT for PTSD and Chronic Pain

Who Can Participate

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • CAPS score of 25 or higher
  • Experienced a single traumatic event
  • Able to understand Swedish
  • Symptoms of chronic pain significantly interfering with everyday life
  • Fully examined medically and received medical treatment if indicated
  • Able to actively participate in rehabilitation and treatment about 5 hours per week
  • Stable dose of medication
  • Able to read and write in Swedish
  • Access to a smartphone or computer with internet
Not Eligible

You will not qualify if you...

  • Experienced repeated and extensive traumatic events
  • Have acute or severe psychiatric disorders or symptoms as primary disorder (e.g., ongoing substance dependence, untreated bipolar disorder, OCD, psychotic symptoms, severe depression)
  • Actively abusing analgesic medications, alcohol, or other drugs
  • Difficulty managing strong emotions leading to outbursts or self-harm
  • Medical health risks
  • Social or economic difficulties or lack of social support hindering behavior change
  • Current severe suicidal thoughts requiring immediate intervention

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Department of Pain Pehabilitation, Skåne University Hospital

Lund, Sweden, 22241

Actively Recruiting

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Research Team

S

Sophia Åkerblom, PhD

CONTACT

S

Sanna Stacke

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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