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Feasibility of a Behavioral Activation Trial

Feasibility of a Behavioral Activation Trial in Community Mental Health

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02992158
Enrollment
80
Registered
2016-12-14
Start date
2016-03-31
Completion date
2019-11-30
Last updated
2020-03-25

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

Conditions

Major Depressive Disorder

Brief summary

The goal of this project is to train community mental health therapists in behavioral activation (BA) treatment for major depressive disorder and then to conduct a study examining the feasibility of evaluating the effectiveness of BA in this setting.

Detailed description

After finalizing a 9-session BA treatment model for major depressive disorder in the Community Mental Health Center (CMHC) setting, the final treatment manual will be used to train clinicians in BA at the CMHC through workshops and training cases. Upon completion of training and certification of adequate implementation of BA, a total of 80 patients with MDD will be randomly assigned in a 3:1 ratio to 9 sessions of BA or treatment-as-usual (TAU) at the CMHC. Feasibility will be assessed in terms of (1) percent of eligible patients who refuse randomization, (2) percent of patients who complete 9 sessions of BA treatment, (3) percent of BA homework assignments that are completed, (4) percent of monthly assessments obtained, and (5) patient ratings of credibility and alliance in BA treatment. The ability of CMHC therapists to adequately implement BA will be assessed by rating taped sessions on BA adherence and competence scales. In addition to feasibility/acceptability of BA and TAU, this study is designed to test whether theoretically important targets of BA change over the course of BA treatment, and whether such changes are associated with changes in depressive symptoms. The target measures will be assessed at baseline, month 1, month 2, and month 3. To support the potential role of these targets as the mechanisms of change in BA, change in the target variables will be examined in relation to change in depression symptoms. The investigators will also pilot a potential moderator of treatment effects (trait reward processing, as measured at baseline using the Effort-Expenditure for Rewards Task) to include this potential moderator in a subsequent fully-powered study with the long-term goal of identifying the types of patients most responsive to BA.

Interventions

BEHAVIORALbehavioral activation
BEHAVIORALtreatment-as-usual

psychotherapy (and potentially medication) as part of treatment-as-usual provided in a community mental health center

Sponsors

Merakey Behavioral Health
CollaboratorUNKNOWN
University of Pennsylvania
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

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

Inclusion criteria

1. confirmed diagnosis of MDD based on the SCID for DSM-IV (or DSM-V, if available), 2. ability to read at least at the 4th grade level, 3. willingness to participate in research, 4. willingness to be audio recorded (for both therapists and patient- participants)

Exclusion criteria

1. current or past psychotic disorder, seizure disorder, or clinically significant organic pathology 2. acute medical problem requiring immediate inpatient treatment, 3. current substance abuse or dependence requiring primary referral to substance abuse program, 4. significant suicidal risk/ideation requiring immediate referral or suicidal gesture within the last 3 months

Design outcomes

Primary

MeasureTime frameDescription
percent of eligible patients who refuse randomizationassessed at baselineWe will calculate this value based on our records of patient participation in baseline assessments.
percent of patients who complete 9 sessions of BA treatment12 weeksWe will calculate this value based on our records of patient attendance of therapy sessions (tracked each week by a research assistant).
percent of BA homework assignments that are completed12 weeksWe will calculate this value based on our records of homework assignment completion (tracked weekly by therapist participants and reported to the research staff).
percent of monthly assessments obtained12 weeksWe will calculate this value based on our records of patient assessment attendance (tracked by a research assistant).
Opinions About Treatment questionnairecollected at week 2This questionnaire measures patient ratings of the credibility of BA treatment.
Brief Alliance Inventorycollected at weeks 2, 4, 6, and 8This questionnaire measures patient ratings of the therapeutic alliance.

Secondary

MeasureTime frame
Dysfunctional Attitudes Scalemonthly for 3 months
Quality of Life Index (questionnaire)monthly for 3 months
Behavioral Activation for Depression Scalemonthly for 3 months
Effort Expenditure for Rewards Task (EEfRT)administered once at baseline and once at month 3
Beck Anxiety Inventorymonthly for three months
Reward Probability Indexmonthly for 3 months
Hamilton Rating Scale for Depressionmonthly for 3 months
Short Form Health Survey (SF-36)monthly for 3 months
Inventory of Depressive Symptomatologymonthly for 3 months
Behavior and Symptom Identification Scale (BASIS-24)monthly for 3 months

Countries

United States

Outcome results

None listed

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