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Acceptance and Commitment Therapy (ACT) Self-help to Reduce Stress

Guided Self-help Based on Acceptance and Commitment Therapy to Reduce Perceived Stress

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03826732
Acronym
ACT
Enrollment
133
Registered
2019-02-01
Start date
2019-01-25
Completion date
2020-05-29
Last updated
2020-09-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stress

Brief summary

The efficacy of guided self-help based on acceptance and commitment therapy (ACT) to reduce subjective sense of stress will be investigated in a randomised controlled trial with two condition: 1) ACT-based self-help, and 2) Wait-list control. The outcome at the end of the treatment (week 10) and 6-month follow-up will be assessed. The wail-list condition will be offered ACT-based self-help after the post-assessment.

Detailed description

The efficacy of guided self-help based on acceptance and commitment therapy (ACT) to reduce subjective sense of stress will be investigated in a randomised controlled trial with two condition: 1) ACT-based self-help, and 2) Wait-list control. The outcome at the end of the treatment and 6-month follow-up will be assessed. The wail-list condition will be offered ACT-based self-help after 10 weeks (i.e. when the post-assessment is completed). Inclusion criteria are: Adults with a score above 14 on the stress sub scale of the Depression, Anxiety, Stress Scale (DASS) at screening, a score below 10 on the Patient Health Questionnaire (PHQ-9), no indication of suicidality on the PHQ-9, and no ongoing psychotherapeutic interventions, and no previous work with the self-help manual that has been published as a self-help book. A total of 140 participants will be recruited and randomised, using services on www.random.org. Informed consent will be obtained from all the participants ahead of screening. Participants will be asked to respond to the following questionnaires at pre-, post and follow-up assessments: Perceived Stress Scale-14 (PSS-14), General Anxiety Disorder-7 (GAD-7), Shirom Melamed Burnout Measure (SMBM), and Brunnsviken Brief Quality of Life Inventory (BBQ). Initially, they will also be asked to respond to the credibility/Expectancy Questionnaire (CEQ). At the end of the intervention (week 10), participants will also be asked to respond to the Client Satisfaction Questionnaire (CSQ), and the Negative Effects Questionnaire (NEQ). The following two scales will be used to study mediators: Acceptance and Action Questionnaire-2 (AAQ-2), and Attention Awareness Scale (MAAS), assess at pre-treatment, as well as at third and fifth week of treatment, at post-assessment (10 weeks later), and at the 6 months follow-up. A number of moderators, including demographics, will also be investigated.

Interventions

BEHAVIORALGuided self-help based on ACT

ACT-based self-help book and regular support by trained facilitators

Sponsors

Karolinska Institutet
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Masking description

Given the nature of the intervention, and self-report as a main strategy for outcome assessment, nor masking is possible or necessary.

Intervention model description

Randomization into active treatment versus a wait-list control group

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Age above 18 * DASS score above 14 * PHQ-9 below 9

Exclusion criteria

* Any indications of suicidality * Any indication of other psychiatric disorder in need of immediate attention/treatment * Concurrent psychotherapy or other treatments for stress * Previous work with the self-help book

Design outcomes

Primary

MeasureTime frameDescription
Perceived Stress Scale-14 (PSS-14)Pre-assessment, week 3 and 5 of intervention, post-assessment (week10), and 6 months follow-upThe PSS-14 is measure of stress. Its total score ranges from 0-56. Lower values represent a better outcome.

Secondary

MeasureTime frameDescription
Patient Health Questionnaire-9 (PHQ-9)Pre- and post-assessment (10 weeks later) as well as 6 months follow-upThe PHQ-9 provides a measure of depressive symptomatology. It ranges from 0-27. Lower values represent a better outcome
General Anxiety Disorder-7 (GAD-7)Pre- and post-assessment (10 weeks later) as well as 6 months follow-upThe GAD-7 is used to measure anxiety. It ranges from 0-21. Lower values represent a better outcome.
Brunnsviken Brief Quality of Life Inventory (BBQ)Pre- and post-assessment (10 weeks later) as well as 6 months follow-upThe BBQ is a Swedish measure of quality of life. It ranges from 0-96. Higher values represent a better outcome.
Shirom Melamed Burnout Measure (SMBM)Pre- and post-assessment (10 weeks later) as well as 6 months follow-upThe SMBM provides a measure of burn-out. It has three sub-scales: 1) physical exhaustion, 2) cognitive fatigue, and 3) emotional exhaustion. The subscales are combined to compute a total score by summing the mean of the subscales. Scale ranges from 3-15. Higher values represent a better outcome.
Mindful Attention Awareness Scale (MAAS)Pre-assessment, week 3 and 5 of intervention, post-assessment (week10), and 6 months follow-upTo measure mindfulness (potential mediator of change). The score is computed by the mean of the 15 items and the resulting scale ranges from 1-6. Higher values represent a better outcome.
Client Satisfaction Questionnaire (CSQ)Post-assessment, and 6 month follow-upTo measure satisfaction and dissatisfaction with the intervention. It ranges from 8-32. Higher values indicate higher satisfaction.
Negative Effects Questionnaire (NEQ)Post-assessment, and 6 month follow-upTo identify iatrogenic events. It ranges from 0-128. Lower values represent a better outcome (i.e. fewer negative effects from the intervention).
Acceptance and Action Questionnaire-2 (AAQ-2)Pre-assessment, week 3 and 5 of intervention, post-assessment (week10), and 6 months follow-upTo Measure psychological flexibility (mediator of change). It ranges from 7-49. Lower values represent a better outcome.

Other

MeasureTime frameDescription
Credibility/Expectancy Questionnaire (CEQ)Pre-assessmentTo measure the perceived credibility of the intervention as well as expectations. It has two subscales; 1) expectancy, and 2) credibility. The individual items are first standardized and then summed up in each subscale. Higher values represent a better outcome.

Countries

Sweden

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026