Telephone Based Cognitive Behavioral Therapy for HIV Related Depression

Depression Clinical Trial

Official title:

Connect: A Pilot Study of Telephone Based Cognitive Behavioral Therapy for HIV Related Depression

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01055158
• Other study ID #: HP-00043648
• Secondary ID: R34MH080630
• Status: Completed
• Phase: N/A
• Start date: January 2010
• Est. completion date: January 2012

Study information

• Verified date: May 2021
• Source: University of Maryland, Baltimore
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to evaluate the effectiveness of a telephone-based, cognitive behavioral therapy intervention in the treatment of depression in adults diagnosed with HIV.

Description:

Up to 40% of individuals receiving medical care for HIV meet DSM-IV criteria for co-occurring depressive disorder. Individuals with HIV and depressive disorders, compared to those with HIV alone, have been shown to have worse adherence to taking antiretroviral medication, increased HIV related morbidity and among women a higher mortality. Previous research suggests that mental health interventions may lead to improved depressive and HIV related outcomes. However because many HIV infected depressed individuals may have trouble accessing mental health services, there is an urgent need for treatment trials to assess whether treatment of depression targeting patients in urban HIV care settings will result in both improved depressive and HIV related outcomes. The goal of this project is to test the preliminary effectiveness of an adapted telephone-based, cognitive behavioral therapy (CBT) intervention targeting HIV infected depressed individuals receiving care in adult outpatient HIV clinics. A total of 60 HIV infected, depressed individuals receiving care at an urban, outpatient HIV clinic will be randomly assigned to receive either the telephone psychotherapy intervention or enhanced usual care with non-specific telephone contact. The results will provide preliminary data on whether the telephone psychotherapy intervention for HIV infected depressed individuals is effective in reducing depression. The results will also be used to determine feasibility, accessibility, and whether the intervention leads to improved retention and better satisfaction.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 38
• Est. completion date: January 2012
• Est. primary completion date: January 2012
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Has a DSM-IV diagnosis of a Depressive Disorder as measured by the mood battery of the MINI

• Has a diagnosis of HIV and is receiving HIV related outpatient care at the Evelyn Jordan Center in Baltimore, MD

• Is able to speak English

• Is able to read English on approximately the 6th grade reading level or higher as measured by the Wide Range Achievement Test 4 (WRAT-4) or by self-report

• Is at least 18 years old

• Has access to a telephone

Exclusion Criteria:

• Meets criteria for dementia by scoring below 10 on the Hopkins HIV Dementia Scale

• Shows signs of serious psychiatric pathology that might either be due to an organic etiology other than HIV, or would generally not be considered treatable solely with psychotherapy, or for whom participation in this protocol might be considered dangerous or unethical

• has a history of serious suicide attempts or is severely suicidal (has ideation, plan, and intent) determined by the MINI

• Patients in psychotherapy are excluded because it is confounded with the study treatments

Related Conditions & MeSH terms

• Depression
• Depressive Disorder
• HIV Infections

Intervention

Behavioral:
• Telephone-based CBT
A form of CBT delivered over the telephone by a trained, licensed, master's or doctoral level clinician. The intervention consists of approximately 10 sessions conducted over approximately 14 weeks. Each session is approximately 30 to 50 minutes. All sessions begin with a depression rating and agenda setting and end with task assignments and summaries.
• Enhanced Usual Care
Participants randomized to this condition will be referred to receive in-person psychotherapy. Research study staff will help participants to set up their first appointment with a psychotherapist.

Locations

Country	Name	City	State
United States	University of Maryland Medical Center, Evelyn Jordan Center	Baltimore	Maryland

Sponsors (3)

Lead Sponsor	Collaborator
University of Maryland, Baltimore	National Institute of Mental Health (NIMH), University of Maryland, College Park

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Hamilton Depression Scale (HAM-D)		Baseline, Week 8, Week 16
Primary	The Quick Inventory of Depressive Symptomatology (16-Item) (Self-Report) (QIDS-SR16)		Baseline, Week 8, Week 16
Secondary	Provision of Social Relationships (PSR)		Baseline, Week 8, Week 16
Secondary	Brief COPE		Baseline, Week 8, Week 16
Secondary	SF-12 Health Survey		Baseline, Week 8, Week 16
Secondary	Therapist Adherence		Week 1-14
Secondary	Participant Adherence to Treatment		Week 1-14
Secondary	Working Alliance Inventory		Week 8, Week 16
Secondary	Satisfaction Index- Mental Health (SIMH-PW)		Week 8, Week 16
Secondary	Expectancy Scales		Week 8, Week 16
Secondary	Adherence to Highly Active Antiretroviral Therapy (HAART)		Baseline, Week 15