Collaborative Care for Depression and Diabetic Retinopathy in African Americans (CC-DDR)

Thomas Jefferson University

Status: Completed

Conditions: Diabetic Retinopathy

Treatments: Behavioral: Behavioral Activation

Study type: Interventional

Funder types: Other

Identifiers

NCT02121340

R34EY024299

Details and patient eligibility

About

In this feasibility/pilot study, we will develop, refine, and evaluate the feasibility of a novel mental health/ophthalmologic intervention called, "Collaborative Care for Depression and Diabetic Retinopathy" (CC-DDR), which aims to treat depression and lower HbA1C in older African Americans with mild-to-moderate diabetic retinopathy (DR) and comorbid depression.

Full description

The Specific Aims are:

1. To develop the CC-DDR treatment protocol. This will involve:

   1. Creating an initial version of the CC-DDR treatment protocol.
   2. Refining the protocol based on input from an expert panel with expertise in DR, depression, and culturally relevant interventions for diabetes in older African Americans.
   3. Developing a tool to assess interventionist treatment adherence and competence.

2. To conduct an open trial of CC-DDR with 40 participants who have poorly controlled diabetes, depression, and mild or moderate DR. During this open trial we will:

   1. Evaluate the feasibility of CC-DDR.
   2. Refine the CC-DDR treatment protocol by incorporating feedback from participants, community health care workers (CHWs), ophthalmologists, and the expert panel.
   3. Refine procedures for recruitment and retention, outcome assessment, monitoring treatment fidelity, CHW training and supervision, quality assurance, and study administration, based on input from investigators, CHWs, participants, and the expert panel.
   4. Examine CC-DDR's impact on depression severity; diabetes self-management practices; HbA1C level; blood pressure; adherence to the ophthalmologist treatment plan; vision function; quality of life; and satisfaction with CC-DDR.

3. To complete a Manual of Procedures that characterizes all aspects of the planned efficacy trial of CC-DDR.

Enrollment: 40 estimated patients

Sex: All

Ages: 65+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. African-American race
2. age ≥ 65 years
3. type 2 diabetes
4. mild or moderate nonproliferative DR with or without macular edema
5. depressive symptoms (i.e., Patient Health Questionnaire-9 score ≥5)
6. HbA1C ≥ 7.0%

Exclusion criteria

1. treated proliferative DR
2. global cognitive impairment (i.e., Mini Mental Status score ≤ 20)
3. psychiatric diagnosis other than depression
4. treatment for depression started in the previous 3 months
5. life expectancy under 2 years

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Single Blind

---

40 participants in 2 patient groups

Behavioral Activation

Experimental group

Description:

CC-DDR is a novel mental health/ophthalmologic intervention that we are designing to treat depression and lower HbA1C levels in older AAs with mild-to-moderate DR and comorbid depression. Community Health Workers, who match participants in race and cultural background, will work with ophthalmologists in the retina clinic to educate participants on the links between depression, HbA1C, and DR, and will extend care into the home where they will use Behavioral Activation to treat depression and improve diabetes self-management skills.

Treatment:

Behavioral: Behavioral Activation

Usual Care

No Intervention group

Description:

Usual Care