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Depression Agency-Based Collaboration

Depression Agency-Based Collaborative (Depression ABC)

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01566318
Enrollment
104
Registered
2012-03-29
Start date
2012-03-31
Completion date
2016-06-30
Last updated
2016-12-13

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

Conditions

Major Depression, Anxiety Disorder

Keywords

Depression, Anxiety, Geriatric mental health

Brief summary

Seniors who receive supportive services face a variety of psychosocial vulnerabilities that put them at risk for depression. One group with very high risk is older adults receiving aging services through Medicaid waiver programs. This 3-year research uses a randomized controlled clinical trial to assess the effectiveness of brief behavioral therapies (problem solving therapy \[PST\] and Brief Behavioral Therapy for Insomnia \[BBTI\]) to prevent depression in seniors receiving aging services.

Detailed description

The research will determine (i) if a course of problem solving therapy (PST) and Brief Behavioral Therapy for Insomnia (BBTI), with boosters, reduces incidence of major depressive episodes over 12 months relative to usual care, and (ii) the extent to which behavioral therapies achieve these effects through enhancement of protective factors, such as greater self-efficacy, better targeting of services to address needs, and greater control over home environments. Periodic blood draws will be used to assess biosignatures of depression. Guiding our investigations of pharmacogenetics, inflammation, and proteomics are synergistic interactions among the serotonergic system, the HPA axis, systemic inflammation, growth factors such as brain derived neuro-trophic factor (BDNF), psychosocial stressors, and vascular co-morbidity. Genetic variation in vasopressin receptors, potentially involved in both cardiovascular risk and social attachment, is also associated with recurrence of depression. Similarly, genetic variation in inflammation may influence antidepressant response and medical co-morbidity.

Interventions

6-8 sessions over 8 weeks, with booster

Sponsors

National Institute of Mental Health (NIMH)
CollaboratorNIH
University of Pittsburgh
Lead SponsorOTHER

Study design

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

Eligibility

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

Inclusion criteria

* Age =\> 60 years * Modified Mini Mental State (3MS) Examination =\>80 * Receiving aging services or difficulty with 1+ ADL/IADL * PHQ-9 score \> 0 and \<= 9 (and question 1 or 2 is \>0)

Exclusion criteria

* Major depressive episode or anxiety disorder within 12 mo * Ever diagnosed with bipolar disorder or schizophrenia * Drug or alcohol use disorder within the past 12 months * Currently taking antidepressants * Currently taking antianxiety med \>4x/week for past 4 weeks

Design outcomes

Primary

MeasureTime frameDescription
Major depressive disorder12 monthsPatient Health Questionnaire score \> 9 with confirming diagnostic interview
Generalized anxiety disorder12 monthsGeneralized anxiety disorder score \>=10, and meets criteria for SCID or PRIME-MD diagnosis

Countries

United States

Outcome results

None listed

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