MedDataX Logo

Guided Internet-delivered Cognitive-behavioral Therapy for Former Chronic Pain Patients

NCT ID: NCT01491269

Last Updated: 2023-12-14

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

72 participants

Study Classification

INTERVENTIONAL

Study Start Date

2009-08-31

Study Completion Date

2010-06-30

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The aim of the present study was to investigate if guided Internet-delivered Cognitive-behavioral Therapy (CBT) would help chronic pain patients who had previously undergone a multidisciplinary treatment but still have residual problems.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

The present study investigates Internet-delivered CBT as a tertiary intervention. This is motivated by the fact that many pain patients relapse after rehabilitation and some may be in need of additional treatment. The persons who fulfills the inclusion criteria undergoes a structured telephone interview. The study is a experimental design with a treatment and an active control group measured before and after a treatment period. The control group were invited to participate in a moderated online discussion forum. Follow up data was collected six months after the treatment.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Chronic Pain

Keywords

Explore important study keywords that can help with search, categorization, and topic discovery.

chronic pain internet delivered CBT tertiary intervention mindfulness applied relaxation guided self help

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Internet delivered CBT

Internet delivered cognitive behavioral intervention, 8 weeks treatment.

Group Type EXPERIMENTAL

Guided Internet-based cognitive behavioural treatment

Intervention Type BEHAVIORAL

Eight weeks internet-based cognitive behavioural treatment. Treatment consisted of education, cognitive skills acquisition, behavioural rehearsal, generalization and maintenance.

No intervention

Waitlist

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

Guided Internet-based cognitive behavioural treatment

Eight weeks internet-based cognitive behavioural treatment. Treatment consisted of education, cognitive skills acquisition, behavioural rehearsal, generalization and maintenance.

Intervention Type BEHAVIORAL

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* to have been medically investigated (within one year)
* completed the multidisciplinary rehabilitation program
* have residual symptoms after the rehabilitation treatment (defined as functional impairment caused by their pain)
* have Internet access

Exclusion Criteria

* planned surgery
* ongoing medical investigation that could impede participation in the study
* suffering from acute physical or psychological conditions
* people confined to wheelchairs
* people not fluent with the Swedish language
Minimum Eligible Age

18 Years

Maximum Eligible Age

65 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Gerhard Andersson

OTHER_GOV

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Gerhard Andersson

professor, Linkoeping University

Responsibility Role SPONSOR_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Gerhard Andersson, Professor

Role: STUDY_DIRECTOR

Linkoeping University

Monica Buhrman, MSc

Role: PRINCIPAL_INVESTIGATOR

Uppsala University

Timo Hursti, PhD

Role: STUDY_CHAIR

Uppsala University

Torsten Gordh, Professor

Role: STUDY_CHAIR

Uppsala University

Anna Fredriksson, MSc

Role: STUDY_CHAIR

Uppsala University

Gunnel Edström, MSc

Role: STUDY_CHAIR

Uppsala University

Dorna Shaffi, MSc

Role: STUDY_CHAIR

Uppsala University

Carolina Törnqvist, MSc

Role: STUDY_CHAIR

Uppsala University

Brjann Ljotsson, PhD

Role: STUDY_CHAIR

Karolinska Institutet, Stockholm

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Uppsala University

Uppsala, , Sweden

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Sweden

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

smartaMB2011

Identifier Type: -

Identifier Source: org_study_id