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NCT Number: NCT06365021

ACT for Syndromic and Subsyndromic Depression in Bipolar Disorder

The goal of this clinical trial is to test the efficacy of Acceptance and Commitment Therapy (ACT) as a psychotherapeutic treatment for patients with Bipolar Disorder (BD). The following questions will be investigated:

* The efficacy of ACT in reducing depressive symptoms in patients with BD. * The efficacy of ACT in improving the quality of life in patients with BD. * The efficacy of ACT in improving functionality in patients with BD. * The efficacy of ACT in improving sleep quality in patients with BD. * The efficacy of ACT in improving psychological flexibility in patients with BD

Participants in the clinical group will undergo 12, 2 hours, weekly sessions of Acceptance and Commitment Therapy, in addition to their regular pharmacological treatment.

Participants in the control group will undergo 3, 2 hours, weekly sessions of Bipolar Disorder Psychoeducation Therapy, in addition to their regular pharmacological treatment.

Scales and assessments will be used to measure study outcomes on 5 different time-points: pre-intervention (month 0), post-intervention (month 3), follow-up 1 (month 6), follow-up 2 (month 9), follow-up 3 (month 12). Mood scales will be assessed every 2 weeks for the duration of treatment and every 4 weeks during the additional 12 week follow-up period.

Results will be compared among both groups to assess the effectiveness of Acceptance and Commitment Therapy as an intervention for syndromic and sub-syndromic depression in bipolar disorder.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Tatiana Cohab Khafif

São Paulo, 01231010, Brazil

Location status: Recruiting

Location contact

Tatiana Khafif, Master's degree

CONTACT

[email protected]

+5511983389643

About this study

Bipolar disorder (BD) is a serious psychiatric disorder characterized by recurrent episodes of mania and depression. The treatment of BD includes a combination of pharmacological medications and psychotherapy to manage episodes and prevent recurrence.

Acceptance and Commitment Therapy (ACT) is an evidence-based psychotherapy. Although there is ample evidence for the efficacy of ACT in the treatment of psychiatric disorders, the literature on ACT for BD is still scarce.There are only five published studies, with three of them being pilot studies.

The present study is justified by the importance to fill a gap in the literature, by aiming to evaluate the effectiveness of ACT as a psychotherapeutic intervention for BD patients and to understand its possible effects mood, quality of life, functionality, sleep, and psychological flexibility on this population.

Main Objective:

To investigate the effectiveness of ACT, in improving syndromic and sub-syndromic depressive symptoms in patients with BD.

Specific objectives:

  • To investigate the efficacy of ACT for improving the quality of life in patients with BD.
  • To investigate the efficacy of ACT in improving functionality in patients with BD.
  • To investigate the efficacy of ACT in improving sleep quality in patients with BD.
  • To investigate the efficacy of ACT in improving psychological flexibility in patients with BD.

Material and Methods:

All participants will be recruited from patients regularly enrolled at the Bipolar Disorder Program - PROMAN - outpatient clinic at Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo. Participants will have access to the Informed Consent Form (ICF), and only those who agree to participate will be included in the study. Randomization Individuals with Bipolar Disorder recruited for the research will be randomized to the ACT arm or Usual Treatment arm through the Online Randomization software.

Procedures:

  • Recruitment will take place in the outpatient clinic of the Bipolar Disorder Program (PROMAN) of the HC-FMUSP Psychiatric Institute and online through the Hospital's social medias.
  • Interested individuals will undergo an initial screening to verify eligibility based on the selection criteria established in the study.
  • Individuals who meet the inclusion criteria will undergo a psychiatric evaluation based on the Standardized Structured Clinical Diagnostic Interview for DSM IV - Axis I Disorders (M.I.N.I.). and complete the initial phase (pre-treatment) instruments via the REDCap platform.
  • Included participants will be randomized into ACT or Psychoeducation group.
  • Participants will be contacted by email or text message with informations regarding the start of treatment.
  • Throughout the intervention, Mood scales (YMRS and MADRS) will be administered periodically (every two weeks)
  • At the end of the intervention, the same assessments administered at baseline will be repeated, as well as at 6, 9 and 12-month follow-ups.

For control purposes, medication changes will be monitored using the MRTF Scale, which allows monitoring of the frequency, type, and reasons for changes in dosages and medications during the intervention protocol. Throughout the study, participants in both groups will continue to receive their usual pharmacological treatment.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Diagnosis of Bipolar Disorder type I and II according to DSM V
  • Presence of depressive symptoms (MADRS>12)
  • Not undergoing psychotherapy
  • Availability to attend in-person group therapy sessions
  • Signing consent form

Exclusion criteria

  • Organic mental disorder
  • Presence of manic or hypomanic symptoms (YMRS>12)
  • Currently undergoing psychotherapy (not able to pause during the study)
  • Major medication change in last 30 days

Treatment and study plan

Acceptance and Commitment Therapy

Behavioral

The ACT protocol for this study was developed by ACT psychologist Tatiana Cohab Khafif specifically for this study and for Bipolar Patients. It is a 12-session protocol that combines psychoeducation elements, mindfulness exercises, experiential exercises, discussions and group processes, homework assignments, and flexible repertoire modeling and training. The protocol is designed to fit into a single trimester. It covers all the basic aspects of Bipolar Disorder and the six processes of ACT.

Other names: ACT

Bipolar Disorder Psychoeducation Therapy

Other

The psychoeducation protocol for this study was developed by clinical psychologist Tatiana Cohab Khafif specifically for this study and for Bipolar Patients. It is a 3-session protocol that combines psychoeducation elements, mindfulness exercises, and discussions regarding the main aspects and symptoms of BD. The protocol is designed to fit into a single month, and has a specifically brief format in order for it not to crossover with psychotherapy. It covers all the basic aspects of Bipolar Disorder.

Primary outcomes

  1. Montgomery-Asberg Depression Scale

    Time frame: Baseline, during treatment every 2 weeks, post-treatment (week 12), in between assessments every 4 weeks, and follow-ups (6, 9 and 12 months)

    Minimum value: 0 (better) Maximum value: 60 (worse)

  2. Young Mania Rating Scale

    Time frame: Baseline, during treatment every 2 weeks, post-treatment (week 12), in between assessments every 4 weeks, and follow-ups (6, 9 and 12 months)

    Minimum value: 0 (better) Maximum value: 54 (worse)

Secondary outcomes

  1. Functional Assessment Staging Tool

    Time frame: Baseline, post-treatment (week 12), and follow-ups (6, 9 and 12 months)

    Minimum value: 0 (better) Maximum value: 72 (worse)

  2. World Health Organization Quality of Life Brief Scale

    Time frame: Baseline, post-treatment (week 12), and follow-ups (6, 9 and 12 months)

    Minimum value: 0 (worse) Maximum value: 100 (better)

  3. Pittsburgh Sleep Quality Index

    Time frame: Baseline, post-treatment (week 12), and follow-ups (6, 9 and 12 months)

    Minimum Value: 0 (better) Maximum Score: 21 (worse)

  4. Psychological Flexibility Questionnaire

    Time frame: Baseline, during treatment weekly, post-treatment (week 12), and follow-ups (6, 9 and 12 months)

    Minimum value: 7 (worse) Maximum value: 49 (better) Higher scores mean a better outcome

Other outcomes

  1. Generalized Anxiety Disorder 7-item Scale

    Time frame: Baseline, post-treatment (week 12), and follow-ups (6, 9 and 12 months)

    Minimum value: 0 (better) Maximum value: 21 (worse)

  2. Medication Recommendation Tracking Form

    Time frame: Baseline, post-treatment (week 12), and follow-ups (6, 9 and 12 months)

    Tracks patient medication use and dosage. There is no score.

  3. Regulatory Satisfaction Alertness Timing Efficiency Duration

    Time frame: Baseline, post-treatment (week 12), and follow-ups (6, 9 and 12 months)

    Minimum Value: 0 (worse) Maximum Value: 18 (better)

Study contacts

Contact information is provided by the study sponsor or research team.

Beny Lafer, MD PhD

CONTACT

[email protected]

+5511 999381849

Tatiana C Khafif, Master's degree

CONTACT

[email protected]

+5511 98338-9643

Sponsors and collaborators

Lead sponsor

Beny Lafer

Other

Registry information

Official study title

Acceptance and Commitment Therapy for Individuals With Syndromic and Subsyndromic Depression in Bipolar Mood Disorder: A Controlled and Randomized Clinical Trial

Important dates

Study start
2024
Primary completion
2025
Study completion
2026
First posted
Apr 15, 2024
Registry last updated
Apr 3, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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