Tatiana Cohab Khafif
São Paulo, 01231010, Brazil
Location status: Recruiting
NCT Number: NCT06365021
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.
Interested in participating?
Request Info18 year–65 year
All sexes
Interventional
Not applicable
São Paulo, 01231010, Brazil
Location status: Recruiting
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:
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:
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
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
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.
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)
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)
Time frame: Baseline, post-treatment (week 12), and follow-ups (6, 9 and 12 months)
Minimum value: 0 (better) Maximum value: 72 (worse)
Time frame: Baseline, post-treatment (week 12), and follow-ups (6, 9 and 12 months)
Minimum value: 0 (worse) Maximum value: 100 (better)
Time frame: Baseline, post-treatment (week 12), and follow-ups (6, 9 and 12 months)
Minimum Value: 0 (better) Maximum Score: 21 (worse)
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
Time frame: Baseline, post-treatment (week 12), and follow-ups (6, 9 and 12 months)
Minimum value: 0 (better) Maximum value: 21 (worse)
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.
Time frame: Baseline, post-treatment (week 12), and follow-ups (6, 9 and 12 months)
Minimum Value: 0 (worse) Maximum Value: 18 (better)
Contact information is provided by the study sponsor or research team.
Beny Lafer, MD PhD
CONTACT
Tatiana C Khafif, Master's degree
CONTACT
Beny Lafer
Other
Acceptance and Commitment Therapy for Individuals With Syndromic and Subsyndromic Depression in Bipolar Mood Disorder: A Controlled and Randomized Clinical Trial
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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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