NCT06816082

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

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
15

participants targeted

Target at below P25 for not_applicable chronic-pain

Timeline
5mo left

Started Jan 2025

Geographic Reach
1 country

1 active site

Status
recruiting

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

Study Progress76%
Jan 2025Oct 2026

First Submitted

Initial submission to the registry

January 10, 2025

Completed
12 days until next milestone

Study Start

First participant enrolled

January 22, 2025

Completed
19 days until next milestone

First Posted

Study publicly available on registry

February 10, 2025

Completed
1.4 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 1, 2026

Expected
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

October 1, 2026

Last Updated

February 10, 2025

Status Verified

January 1, 2025

Enrollment Period

1.4 years

First QC Date

January 10, 2025

Last Update Submit

February 3, 2025

Conditions

Keywords

chronic painacceptance and commitment therapyinternet delivered treatment

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

EXPERIMENTAL

7 week long treatment with therapist asynchronous support in mainly text format. Treatment includes for example mindfulness, psychoeducation, values, and self-compassion

Behavioral: Internet delivered acceptance and commitment therapy

Interventions

7 week long treatment with therapist asynchronous support in mainly text format. Treatment includes for example mindfulness, psychoeducation, values, and self-compassion

Internet delivered acceptance and commitment therapy

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

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

RECRUITING

MeSH Terms

Conditions

Chronic Pain

Condition Hierarchy (Ancestors)

PainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Nina Bendelin, PhD

    Region Östergötland

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Nina Bendelin, PhD

CONTACT

Peter Molander, PhD

CONTACT

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

Locations