search
Back to results

Internet-delivered ACT for Chronic Pain (iACT)

Primary Purpose

Chronic Pain

Status
Completed
Phase
Not Applicable
Locations
Sweden
Study Type
Interventional
Intervention
Internet delivered Acceptance and Commitment therapy
Waiting list control condition
Sponsored by
Rikard Wicksell
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Pain

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • a pain duration of ≥ 6 months;
  • are able to communicate in Swedish
  • have access to computer and internet in their home environment.
  • have access to a cell phone with the possibility of receiving text messages
  • no planned changes in medication use, or any other changes in interventions for their pain planned

Exclusion Criteria:

  • injury or illness that require immediate assessment or different treatment, or that is expected to progress significantly during the next 6 months
  • unstable medication (planned changes in medication during next 4 months)
  • previous ACT or CBT treatment during the past 3 months
  • severe psychiatric co-morbidity (e.g. high risk of suicide) as assessed by the psychologist in a semi-structured interview

Sites / Locations

  • Karolinska Institutet

Arms of the Study

Arm 1

Arm 2

Arm Type

Other

Other

Arm Label

Treatment

Waiting list control condition

Arm Description

Internet delivered Acceptance and Commitment therapy, supported by a psychologist/psychology student under supervision.

Participants receive no treatment for ten weeks, i.e. waiting list condition. Following post-assessment, the control condition receive unguided iACT (i.e. the same content and structure as iACT but without systematic therapist communication).

Outcomes

Primary Outcome Measures

Pain Interference Index (changes between assessments)
Self rated measure of daily functioning related to pain

Secondary Outcome Measures

The Valuing Questionnaire (changes)
Self rated progress and obstacles in valued actions
Psychological Inflexibility in Pain Scale (changes)
Self rated psychological inflexibility related to pain
Patient Health Questionnaire 9 (changes)
Self rated depressive symptoms
European Quality of Life Five Dimensions Questionnaire (changes)
Self rated quality of life
Insomnia Severity Index (changes)
Self rated degree of insomnia
Pain Intensity (changes)
Self rated degree of pain during the last week on a scale from 0-10
Occupational status (changes)
Self reported occupational status indicated on a pre specified list, including sick leave and/or retirement
Perceived Stress Scale - 4 items (changes)
Self rated level of perceived stress
General Anxiety Disorder - 7 item (changes)
Self rated symptoms of general anxiety
Medication use (changes)
Self reported medicine use

Full Information

First Posted
March 15, 2017
Last Updated
January 1, 2019
Sponsor
Rikard Wicksell
Collaborators
AFA Insurance
search

1. Study Identification

Unique Protocol Identification Number
NCT03105908
Brief Title
Internet-delivered ACT for Chronic Pain
Acronym
iACT
Official Title
Internet-delivered ACT Treatment for Patients With Chronic Pain: A Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
January 2019
Overall Recruitment Status
Completed
Study Start Date
March 16, 2017 (Actual)
Primary Completion Date
October 31, 2018 (Actual)
Study Completion Date
October 31, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Rikard Wicksell
Collaborators
AFA Insurance

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The overall aim of the present study is to evaluate an internet-delivered Acceptance and Commitment therapy treatment (iACT) for patients with chronic pain. More specifically, the study will evaluate if 1) iACT is effective in improving functioning and quality of life in comparison to a waitlist condition, 2) if iACT is cost-effective, 3) factors that influence treatment outcome (i.e. predictors, moderators or characteristics of treatment responders), 4) if psychological variables mediates the effects of treatment on outcome, and 5) if subgroups of patients varies in change processes (i.e. moderated mediation). The main hypothesis is that iACT will improve functioning and quality of life.
Detailed Description
Chronic pain affects 12-30% of the population and often results in depression, disability, and reduced quality of life. Medical strategies are often ineffective or insufficient to alleviate symptoms and increase functioning. Instead, the empirical support for cognitive behavior therapy (CBT) is today well established, and such interventions are commonly seen as critically important for patients with chronic pain. However, modest effects sizes calls for further improvements. Recent developments within CBT, particularly Acceptance and Commitment Therapy (ACT), have suggested the utility of acceptance and mindfulness strategies to manage pain and distress. The body of evidence for ACT has grown rapidly during the past decade, and ACT is today listed by the American Psychological Association as a treatment for chronic pain, with strong empirical support. Internet-delivered ACT Despite the increased empirical support for ACT the availability is still very limited, and a large number of patients do not receive this treatment. In other domains, the accessibility of empirically supported treatments has increased during the past decade due to the development of methods to deliver the treatment via internet. For example, a large number of studies illustrate the utility of internet-delivered CBT for anxiety, insomnia and depression, with treatment effects similar to those obtained in studies with face-to-face treatment. Few studies have yet evaluated internet-delivered ACT (iACT) for chronic pain, but a recent pilot study from our group with participants suffering from fibromyalgia (n=41) illustrated very promising results that warrant further studies to evaluate the effects of this treatment. Moderators and mediators of treatment outcome If iACT shows to be effective, it is vital to identify for whom this treatment works. For example, it is possible that factors such as age, pain duration or depression may moderate the effects of treatment. Also, it is likely that some individuals who respond well to regular face-to-face treatment do not benefit from internet-delivered interventions. Furthermore, recent studies have shown that acceptance of pain and distress may be a more important mediator of change than e.g. pain intensity, catastrophizing or anxiety. However, no study has to our knowledge yet explored if subgroups of patients (e.g. men and women) improve via different change processes (i.e. moderated mediation). More information regarding moderators and mediators of change will make it possible to adjust and tailor interventions to meet specific individual needs, and thereby increase the effects of treatment. Recruitment Patients will be recruited through self referral. Thus, information regarding the study will be provided through newspapers and social media, as well as in direct communication with pain clinics and primary care units, including instructions regarding e.g. eligibility and how to sign up. Once patients have been found eligible and expressed interest in study participation they will be assessed by a psychologist, and when needed by a pain physician, via semi-structured interviews to confirm eligibility and to ensure that the patient meet the study criteria. Informed consent is obtained from all participants prior to the assessment. Statistical methods Evaluations of treatment effects are primarily based on intent-to-treat analyses. The statistical approach will primarily be based on linear multilevel modeling (LMM), which takes into account dependencies between repeated measures and differences between patients in pre-treatment status and treatment response (i.e. random effects modeling) and also provide means of handling missing data. More traditional methods, such as ANOVA and hierarchical regression, may also be utilized when appropriate. Analyses of change processes (mediation, moderation, moderated mediation) will follow guidelines and recommendations (e.g. cross-product of coefficients approach, bootstrapping). The main health economic outcomes will be the incremental cost-effectiveness ratio, which is a measure of the relationship between the cost of the treatment and the incremental value it provides in terms of functioning, compared to the control condition.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Pain

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
113 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Treatment
Arm Type
Other
Arm Description
Internet delivered Acceptance and Commitment therapy, supported by a psychologist/psychology student under supervision.
Arm Title
Waiting list control condition
Arm Type
Other
Arm Description
Participants receive no treatment for ten weeks, i.e. waiting list condition. Following post-assessment, the control condition receive unguided iACT (i.e. the same content and structure as iACT but without systematic therapist communication).
Intervention Type
Behavioral
Intervention Name(s)
Internet delivered Acceptance and Commitment therapy
Other Intervention Name(s)
iACT
Intervention Description
The main component in the treatment is exposure to symptoms and feared situations. The iACT program is adapted from the evidence based face-to-face treatment at the Behavioral Medicine unit at Karolinska University Hospital. The iACT program has a different structure but is equal in content to face-to-face treatment, and is to be completed within ten weeks. Participants receive texts, audio files, movies and exercises and have online contact with their psychologist via an internet platform or a smart phone application. The treatment aims to encourage valued behaviors in the presence of inner discomfort.
Intervention Type
Behavioral
Intervention Name(s)
Waiting list control condition
Intervention Description
After a ten week wait list period, the control condition receive same treatment as the intervention group, but without therapist support.
Primary Outcome Measure Information:
Title
Pain Interference Index (changes between assessments)
Description
Self rated measure of daily functioning related to pain
Time Frame
Baseline, 10 weekly ratings, post (10 weeks), follow ups three, six and twelve months post treatment
Secondary Outcome Measure Information:
Title
The Valuing Questionnaire (changes)
Description
Self rated progress and obstacles in valued actions
Time Frame
Baseline, mid (4 weeks), post (10 weeks), follow ups three, six and twelve months post treatment
Title
Psychological Inflexibility in Pain Scale (changes)
Description
Self rated psychological inflexibility related to pain
Time Frame
Baseline, 10 weekly ratings, post (10 weeks), follow ups three, six and twelve months post treatment
Title
Patient Health Questionnaire 9 (changes)
Description
Self rated depressive symptoms
Time Frame
Baseline, post (10 weeks), follow ups three, six and twelve months post treatment
Title
European Quality of Life Five Dimensions Questionnaire (changes)
Description
Self rated quality of life
Time Frame
Baseline, post (10 weeks), follow ups three, six and twelve months post treatment
Title
Insomnia Severity Index (changes)
Description
Self rated degree of insomnia
Time Frame
Baseline, post (10 weeks), follow ups three, six and twelve months post treatment
Title
Pain Intensity (changes)
Description
Self rated degree of pain during the last week on a scale from 0-10
Time Frame
Baseline, post (10 weeks), follow ups three, six and twelve months post treatment
Title
Occupational status (changes)
Description
Self reported occupational status indicated on a pre specified list, including sick leave and/or retirement
Time Frame
Baseline, post (10 weeks), follow ups three, six and twelve months post treatment
Title
Perceived Stress Scale - 4 items (changes)
Description
Self rated level of perceived stress
Time Frame
Baseline, post (10 weeks), follow ups three, six and twelve months post treatment
Title
General Anxiety Disorder - 7 item (changes)
Description
Self rated symptoms of general anxiety
Time Frame
Baseline, post (10 weeks), follow ups three, six and twelve months post treatment
Title
Medication use (changes)
Description
Self reported medicine use
Time Frame
Baseline, post (10 weeks), follow ups three, six and twelve months post treatment

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: a pain duration of ≥ 6 months; are able to communicate in Swedish have access to computer and internet in their home environment. have access to a cell phone with the possibility of receiving text messages no planned changes in medication use, or any other changes in interventions for their pain planned Exclusion Criteria: injury or illness that require immediate assessment or different treatment, or that is expected to progress significantly during the next 6 months unstable medication (planned changes in medication during next 4 months) previous ACT or CBT treatment during the past 3 months severe psychiatric co-morbidity (e.g. high risk of suicide) as assessed by the psychologist in a semi-structured interview
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rikard Wicksell, PhD, MSc
Organizational Affiliation
Karolinska Institutet
Official's Role
Principal Investigator
Facility Information:
Facility Name
Karolinska Institutet
City
Stockholm
State/Province
Stockholms Län
ZIP/Postal Code
171 77
Country
Sweden

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Internet-delivered ACT for Chronic Pain

We'll reach out to this number within 24 hrs