Internet-based Acceptance Based Psychotherapy As an Adjunct to Chronic Pain Rehabilitation
1 other identifier
interventional
15
1 country
1
Brief Summary
The goal of this clinical trial is to evaluate how an acceptance based internet-delivered psychological treatment (IACT) tailored to patients with chronic pain is perceived, and if it meets the needs and expectations of those enrolled. The main question it aims to answer is: What are the expectations of patients with chronic pain prior to IACT treatment, and how do they experience IACT during and after treatment? Participants will be offered a 7 week long treatment with therapist support. They will be interviewed before treatment starts, once during treatment, and again after treatment is completed.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable chronic-pain
Started Jan 2025
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
January 10, 2025
CompletedStudy Start
First participant enrolled
January 22, 2025
CompletedFirst Posted
Study publicly available on registry
February 10, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 1, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
October 1, 2026
February 10, 2025
January 1, 2025
1.4 years
January 10, 2025
February 3, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Main outcome - qualitative
Semi-structured interviews with patients experiencing chronic pain will be conducted before, during, and after IACT treatment. The interviews will be analyzed thematically to identify recurring themes related to patients' expectations of IACT treatment, their experiences during the treatment, their perceptions of the treatment, and the extent to which the treatment meets their needs. The main areas that will be explored include, but are not limited to, expectations regarding function, pain perception, and quality of life; experiences of the treatment process; perceived benefits and drawbacks of the treatment; and perceptions of whether the treatment addressed their individual needs.
Before treatment starts, once in the middle of treatment (3 weeks after start), and after treatment has ended (at 7 weeks post start).
Secondary Outcomes (10)
Quantitative - Brief Pain Inventory
Pre and post (7 weeks)
Quantitative - Chronic Pain Acceptance Questionnaire 8
pre and post (7 weeks)
Quantitative -Pain Self-Efficacy Questionnaire 8
pre and post (7 weeks)
Quantitative - Pain Catastrophizing Scale
pre and post (7 weeks)
Quantitative - Numeric rating scale
Pre and post (7 weeks)
- +5 more secondary outcomes
Study Arms (1)
Internet delivered acceptance and commitment therapy
EXPERIMENTAL7 week long treatment with therapist asynchronous support in mainly text format. Treatment includes for example mindfulness, psychoeducation, values, and self-compassion
Interventions
7 week long treatment with therapist asynchronous support in mainly text format. Treatment includes for example mindfulness, psychoeducation, values, and self-compassion
Eligibility Criteria
You may qualify if:
- Participants must be adults with sufficient understanding of Swedish to speak and read, have internet access, and currently be a patient at the Pain and Rehabilitation Clinic in Linköping.
You may not qualify if:
- Severe cognitive problems, or severe mental illness such as a psychotic episode
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Pain and Rehabilitation Clinic
Linköping, Östergötland County, 58758, Sweden
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Nina Bendelin, PhD
Region Östergötland
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER GOV
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Lic Psychologist, Clinical Researcher, PhD
Study Record Dates
First Submitted
January 10, 2025
First Posted
February 10, 2025
Study Start
January 22, 2025
Primary Completion (Estimated)
July 1, 2026
Study Completion (Estimated)
October 1, 2026
Last Updated
February 10, 2025
Record last verified: 2025-01