Internet-delivered ACT for emotional distress and chronic pain

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This pilot study will test an internet-based ACT program designed to reduce emotional distress in adults with chronic pain. Participants receive education on distress and pain, plus exercises targeting mindfulness, cognitive defusion, and acceptance, delivered through a secure online platform. Two planned telephone contacts with a psychologist and a platform message system provide support, with responses within 48 hours. Assessments occur at baseline, immediately after treatment (2 weeks), and at a 3-month follow-up to evaluate changes in distress and pain-related outcomes.

Why it matters

Who can join: the full rules

Inclusion Criteria:

emotional distress characterized by clinically significant symptoms of anxiety or depression age between 18-65 years 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 patient at department of pain rehabilitation, SUS

Exclusion Criteria:

had 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, PTSD) 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)

Where it's running

• Department of pain rehabilitation
  Lund, Sweden Recruiting

Study contacts

• Study coordinator: Sophia Åkerblom, Associate professor
• Email: sophia.akerblom@skane.se
• Phone: 004646172610

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.