The overall goals of the proposed research study are to: (1) examine quantitative outcomes in a well-conducted randomized clinical trial of Calmer Life, relative to Enhanced Community Care, an information and referral intervention that represents care in a real-world community-service environment, and (2) evaluate implementation feasibility, which includes training community providers; examining program reach, engagement, acceptability, and barriers-facilitators; and preparing practical tools for replicating the program.
Cognitive behavioral treatment (CBT) produces positive outcomes for late-life worry/GAD in academic and primary care settings, but minorities are significantly underrepresented in clinical trials, and standard CBT poorly addresses the needs of low-income minority older adults in underserved communities. More attention needs to be given to service delivery of anxiety treatments for underserved older adults. Calmer Life (CL) is a culturally tailored, participant-centered research study that offers a skills-based intervention for late-life anxiety and includes other elements of care to meet the needs of underserved, minority older adults, including the option to integrate religion/spirituality (R/S), flexible delivery modes, and modular treatment format. Participants will be randomly assigned to CL or Enhanced Community Care(ECC). CL and ECC will be provided by behavioral health clinicians recruited from partner organizations, psychology trainees, and other research staff over 3 months. Assessments will occur at baseline and 3 months. Participants in the CL condition can choose up to 12 individual skill sessions, and will be recommended to complete a minimum of 6 sessions. If participants desire to incorporate R/S, an R/S assessment occurs during session 2 to help the provider understand the participant's beliefs and practices. R/S can be integrated into any of the skills learned during the intervention (e.g., deep breathing, self-statements, sleep management) or omitted entirely. Participants in the ECC condition will receive brief biweekly check in calls to provide information about community resources (including mental health), offer emotional support, and assess symptom severity and need for crisis intervention. Emergency procedures will be followed in crisis situations. After 3 months of ECC is completed, participants in the ECC group will be offered the CL intervention. Outcome measures will be administered for participants in both groups at baseline, 1 month, and 3 months. Participants in ECC will complete measures at 6 months after completion of CL.
Study Type
INTERVENTIONAL
Houston Center for Quality of Care and Utilization Studies
Houston, Texas, United States
Geriatric Anxiety Inventory
Time frame: 3 months
Penn State Worry Questionnaire (PSWQ-A)
Time frame: 3 months
Generalized Anxiety Disorder-7
Time frame: 3 months
Patient Health Questionnaire-9
Time frame: 3 months
Insomnia Severity Index
Time frame: 3 months
Late-Life Functional Disability Index
Time frame: 3 months
SF-12 Health Survey
Time frame: 3 months
Client Satisfaction Questionnaire
Time frame: 3 months
Brief RCOPE
Religious coping
Time frame: 3 months
Health services use
Time frame: 3 months
Use of psychotropic medication
Time frame: 3 months
Brief Multidimensional Measure of Religiousness and Spirituality
Time frame: 3 months
Satisfaction with Life Scale
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Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
60
Time frame: 3 months
Geriatric Depression Scale
Time frame: 3 months