Personalized Indications for CBT and Antidepressants in Treating Depression

PHASE4RecruitingINTERVENTIONAL
Enrollment

80

Participants

Timeline

Start Date

October 31, 2016

Primary Completion Date

June 30, 2026

Study Completion Date

June 30, 2027

Conditions
Major Depressive DisorderPersistent Depressive Disorder
Interventions
BEHAVIORAL

Cognitive Behavioral Therapy

CBT will be delivered in a one-to-one face-to-face format by trained Masters or PhD level CBT therapists who will follow a protocol adapted from existing manuals and piloted in the participating centres. Up to 20 sessions will be offered over 18 weeks, initially twice per week, then weekly and later spaced to every other week. The treatment will have core obligatory modules and flexible elements adaptable to participant's maintaining factors.

DRUG

Pharmacotherapy

Pharmacotherapy will be prescribed and adjusted by psychiatrists in 20-30 minute pharmacotherapy sessions once every two weeks. The manual-guided best-evidence pharmacotherapy will follow current guidelines for first, second and third line treatment.41 The primary focus will be on serotonin-reuptake inhibiting antidepressant (escitalopram 5-20mg, sertraline 50-200 mg daily) monotherapy, which may remain the only treatment for the majority of participants. Augmentation (aripiprazole 2-10mg, bupropione 150-450mg) will be offered to participants with partial response. The manual, developed as part of Canadian Biomarker Integration Network in Depression (CAN-BIND).43, also specifies admissible supportive therapeutic elements and prohibits CBT-specific techniques.

Trial Locations (1)

B3H 2E2

RECRUITING

Nova Scotia Health Authority, Halifax

All Listed Sponsors
collaborator

University Health Network, Toronto

OTHER

collaborator

Queen's University

OTHER

collaborator

Centre for Addiction and Mental Health

OTHER

lead

Nova Scotia Health Authority

OTHER