CClinicalTrials.gg
CompletedNCT06900608Updated Mar 28, 2025

Targeted ACT Compared to Supportive Therapy for Depression RCT

An interventional study of Acceptance and Commitment Therapy and Treatment as usual in Acceptance and Commitment Therapy and Supportive Therapy, sponsored by Western Michigan University. Completed. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2025-03-28.

Sponsored by Western Michigan University · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 15 years 1 month after the study started (first participant enrolled Feb 2010, registered Mar 2025).
Phase
Not applicable
Study type
Interventional
Enrollment
52
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

Acceptance and Commitment Therapy (ACT) has demonstrated efficacy in reducing depressive symptoms, primarily compared to no treatment or minimal treatment controls. This study compared the efficacy of ACT targeting cognitive defusion (CD, 3 sessions) and values-based activity scheduling (VBAS, 3 sessions) to supportive therapy (ST). Both treatments offered six sessions, a rationale for the approach, related techniques, and homework assignments. A parallel group randomized controlled efficacy trial design was used. Participants were stratified by gender identification and depression severity and then randomly allocated, according to a predetermined sequence, 2:1 to ACT or ST. Dependent measures were collected during acute treatment (pre, mid, and post-treatment) and follow-up at one-month.

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Conditions studied

  • Acceptance and Commitment Therapy
  • Supportive Therapy
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In context

Lead sponsor

Western Michigan University is the lead sponsor of 9 studies on the registry; 2 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • 18 years or older
  • Scored one SD below the mean on the RSES and BSI
  • Proficiency in English
  • If taking medication for psychiatric reasons, stable medication use for at least eight weeks prior to enrollment and agreement to no changes in dosing during study participation.

Exclusion criteria

Exclusion Criteria:

  • Receiving other forms of psychological treatment
  • Meeting PDSQ Interview criteria for psychosis, panic disorder, substance use, or endorsement of significant suicidal ideation
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Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Outcomes assessor)
Enrollment
52 participants (actual)

Study arms

  • Experimental
    Acceptance and Commitment Therapy

    Behavioral: Acceptance and Commitment Therapy

  • Active comparator
    Supportive Therapy

    Behavioral: Treatment as usual

Interventions

  • BehavioralAcceptance and Commitment Therapy

    A 6-session ACT intervention was implemented targeting Cognitive Defusion (CD) and Values-Based Activity Scheduling (VBAS). During the first 3 sessions, the therapist taught participants how to defuse from negative self-thoughts using didactic and experiential techniques and emphasized the relationship between negative thoughts and the self and learning to observe negative thoughts for what they are - thoughts, words, ideas, and evaluations. During sessions 4-6, the therapist used similar techniques to focus on behaving in meaningful ways without letting negative thoughts dictate behavior. During these VBAS sessions, the participant identified their values and worked with the therapist to decide on goals that were values-consistent, and focused on those foals without letting negative thoughts and emotions get in the way of living toward them.

  • BehavioralTreatment as usual

    The 6-session supportive therapy (ST) condition emphasized the exploration of feelings; helping the client to become aware of and talk about emotional experiences with no attempt to change thoughts, behaviors, or the client's experiences directly (Greenberg et al., 1998). Psychoeducation emphasized the untoward effects of not acknowledging or exploring feelings and benefits of identification and talking about feelings. The therapist used open-ended questions, reflective listening, empathy, and clarification questions. Therapists did not give advice, offer solutions, make interpretations, or disagree with/confront the client. For homework, the participants were asked to complete "awareness homework," involving monitoring of presence, intensity, and duration of emotions with no prescription to change them or do anything differently.

    Also known as: Supportive Therapy

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What researchers measure

Primary outcomes

  1. Demographic Questionnaire

    Time frame: Pre-treatment

  2. Rosenberg Self-Esteem Scale

    The Rosenberg Self-Esteem Scale (RSES) is a 10-item scale asking participants to rate their level of agreement (on a scale 0-4) with statements describing general feelings about themselves. Higher scores represent a more positive self-evaluation. Scores range from 0 to 40.

    Time frame: Pre-treatment, 3 weeks, 6 weeks/post-treatment, and 1 month after post-treatment

  3. Brief Symptom Inventory-Global Severity Index

    The Brief Symptom Inventory-Global Severity Index (BSI) is a 53-item questionnaire that provides an overview of psychological symptoms and their severity. Items are endorsed on a Likert scale (0-not at all to 4-extremely) with higher scores indicating higher rates of general distress. Scores can range from 0 to 212.

    Time frame: Pre-treatment, 3 weeks, 6 weeks/post-treatment, and 1 month after post-treatment

  4. Psychiatric Diagnostic Screening Questionnaire (PDSQ)

    The Psychiatric Diagnostic Screening Questionnaire (PDSQ) consists of a) 125 item "yes/no" screener used to assess for symptoms of 13 psychopathologies and b) semi-structured interview(s) as indicated by endorsement of scores above the cut-off on any given psychopathology subscale based on the 125-item screener. Participants whose interview for major depressive disorder was positive for 2-4 symptoms were considered to meet criteria for minor depression, while those with 5-9 symptoms were considered to meet criteria for major depressive disorder. Each "yes" indicates one symptom, with a range of 0-9 symptoms within the depressive disorder category.

    Time frame: Pre-treatment, 3 weeks, 6 weeks/post-treatment, and 1 month after post-treatment

  5. Beck Depression Inventory - II (BDI)

    The Beck Depression Inventory - II (BDI) is a 21-item self-report scale assessing the severity of depressive symptoms. Higher scores indicate higher rates of depressive symptoms and intensity, with scores ranging from 0-63.

    Time frame: Pre-treatment, 3 weeks, 6 weeks/post-treatment, and 1 month after post-treatment

  6. Acceptance and Action Questionnaire - II (AAQ-II)

    The Acceptance and Action Questionnaire - II (AAQ-II) is a 7-item scale measuring experiential avoidance and psychological flexibility. Each item is scored on a 1 (never true) - 7 (always true) scale with higher scores indicate greater inflexibility. Scores range from 7-49.

    Time frame: Pre-treatment, 3 weeks, 6 weeks/post-treatment, and 1 month after post-treatment

  7. Automatic Thoughts Questionnaire (ATQ)

    The Automatic Thoughts Questionnaire (ATQ) contains 30-items measuring the frequency and believability of negative self-statements, with higher scores indicating higher frequency or believability of thoughts. Each item is scored on a 1-5 scale (ranging from "not at all" to "all the time"), with total score ranging from 30-150.

    Time frame: Pre-treatment, 3 weeks, 6 weeks/post-treatment, and 1 month after post-treatment

  8. Environmental Reward Observation Scale (EROS)

    The Environmental Reward Observation Scale (EROS) consists of 10 items using a 4-point Likert scale (1 = strongly disagree, 4 = strongly agree) assessing whether affect and behavior increases as a result of contact with positively rewarding activities. Higher scores indicate larger increases when in contact with positively rewarding activities. Total scores range from 10-40.

    Time frame: Pre-treatment, 3 weeks, 6 weeks/post-treatment, and 1 month after post-treatment

  9. Valued Living Questionnaire (VLQ)

    The Valued Living Questionnaire (VLQ) is a 20-item self-report measure. Participants' rate, on a scale of 1-10, first the importance of values in 10 domains (e.g., family, work, education, relationships) and then the consistency of action taken towards those values during the last week. When used as an omnibus measure the VLQ is scored by taking the mean of the products of the Importance and Consistency ratings. Higher scores indicate higher consistency or higher importance of each value. Total scores can range from 10-100.

    Time frame: Pre-treatment, 3 weeks, 6 weeks/post-treatment, and 1 month after post-treatment

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Study locations

No study locations are listed for this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 28, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT06900608
Lead sponsor
Western Michigan University
Responsible party
Sponsor
First posted
Mar 28, 2025
Start date
Feb 1, 2010
Primary completion
Dec 30, 2011
Completion
Dec 31, 2011
Last update
Mar 28, 2025

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Mar 2025. You cannot join it, but the record below documents what was studied.

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