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Cognitive Behavioral Therapy for Depression (CBT Trial)

N/A
Waitlist Available
Research Sponsored by Northwestern University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up post-treatment which is within 2 weeks after final therapy session (i.e. estimated 12-14 weeks after initial intake interview)
Awards & highlights

Summary

This trial tests a new, easier-to-understand therapy called Adapted Cognitive-Behavior Therapy (ACBT) for women with depression who have trouble reading. The goal is to see if ACBT works better than regular therapy for these women.

Who is the study for?
This trial is for English-speaking women over 18 with major depressive disorder who are willing to try different types of therapy and complete all study assessments. They must not plan to move from the Chicagoland area during the study, have no severe substance use disorders, suicidal actions in recent months, or significant neurological diseases.
What is being tested?
The trial compares Adapted Cognitive-Behavior Therapy (ACBT), designed for those with low literacy, against standard Cognitive Behavior Therapy (CBT) to see which is more effective at improving outcomes for women suffering from depression.
What are the potential side effects?
While CBT typically doesn't cause physical side effects, participants may experience emotional discomfort discussing personal issues. Some might feel anxious or upset temporarily after sessions.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~post-treatment which is within 2 weeks after final therapy session (i.e. estimated 12-14 weeks after initial intake interview)
This trial's timeline: 3 weeks for screening, Varies for treatment, and post-treatment which is within 2 weeks after final therapy session (i.e. estimated 12-14 weeks after initial intake interview) for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
PROMIS Depression: : 3-month follow-up (defined as 3 months after the last (i.e., 12th) session of cognitive behavior therapy.
PROMIS Depression: Post-treatment (defined as completing 12 therapy session)
Secondary study objectives
World Health Organization Disability Assessment Schedule 2.0 (WHODAS 2.0): 3-month follow-up (defined as 3 months after the end of treatment)
World Health Organization Disability Assessment Schedule 2.0 (WHODAS 2.0): Post-treatment (defined as completing 12 sessions of therapy; this will occur an estimated 12-14 weeks after initial intake interview)
Other study objectives
California Psychotherapy Alliance Scale - Participant version short-form - Post-treatment (defined as completing 12 sessions of therapy; this will occur an estimated 12-14 weeks after initial intake interview)
Patient Global Impression of Change (PGIC) 3-month follow-up (defined as 3 months after the end of treatment)
Patient Global Impression of Change (PGIC): Post-treatment (defined as completing 12 sessions of therapy; this will occur an estimated 12-14 weeks after initial intake interview)

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: Adapted CBTExperimental Treatment1 Intervention
Adapted CBT, 12 sessions each lasting 45 minutes
Group II: Standard CBTActive Control1 Intervention
Standard CBT, 12 sessions each lasting 45 minutes
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Adapted CBT
2020
N/A
~30

Research Highlights

Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.
Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Cognitive-Behavioral Therapy (CBT) helps depression patients by identifying and modifying negative thought patterns and behaviors. Adapted Cognitive-Behavior Therapy (ACBT) tailors this approach for individuals with low literacy, using simpler language and methods to ensure better understanding and engagement. This inclusivity is crucial as it makes effective treatment accessible to a broader range of patients, potentially improving their outcomes.

Find a Location

Who is running the clinical trial?

Northwestern UniversityLead Sponsor
1,625 Previous Clinical Trials
937,267 Total Patients Enrolled
67 Trials studying Depression
27,974 Patients Enrolled for Depression
~4 spots leftby Sep 2025