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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT06170255
Other study ID # 5K23HL109620
Secondary ID
Status Completed
Phase Phase 1/Phase 2
First received
Last updated
Start date March 6, 2014
Est. completion date October 2, 2017

Study information

Verified date December 2023
Source East Carolina University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study was designed to determine the feasibility of a Randomized Controlled Trial (RCT) that involved treating depression among participants with an elevated risk for cardiovascular disease. It is expected that treating depression through non-pharmacological means will impact heart rate variability, a proximal measure of CVD risk.


Recruitment information / eligibility

Status Completed
Enrollment 16
Est. completion date October 2, 2017
Est. primary completion date October 2, 2017
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 21 Years to 75 Years
Eligibility Inclusion Criteria: Males and females age 21-75 Meet diagnostic criteria for major depressive disorder Framingham risk score indicating a greater than negligible 10-year risk (3% or greater) for cardiovascular disease. Levels of depressive symptoms of at least moderate level (beck depression inventory II score > 19 of 63 possible points; or a Hamilton depression rating scale > 12 of 50 possible points) Exclusion Criteria: A verbal expression of current, significant, suicidal ideation; a score of > 15 on the beck scale for suicidal ideation Score of >1 on any single item of the Beck Scale for Suicidal Ideation Score of > 1 on the item assessing suicidal ideation on the beck depression inventory II. Psychiatric diagnoses that could potentially interfere with depression treatment (current post traumatic stress disorder, bipolar I disorder, obsessive-compulsive disorder, bulimia or anorexia nervosa, schizophrenia, and panic disorder) Current use of an antidepressant medication Currently in psychotherapy. Current use of a beta blocker, anxiolytic (benzodiazepine), antipsychotic agent Diagnosis of CVD.

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Behavioral Activation (BA)
Behavioral activation involves an exploration of the patient's individualized values and follows with goal setting to improve depression symptoms.

Locations

Country Name City State
n/a

Sponsors (3)

Lead Sponsor Collaborator
East Carolina University National Heart, Lung, and Blood Institute (NHLBI), National Institute of Mental Health (NIMH)

Outcome

Type Measure Description Time frame Safety issue
Primary Feasibility Feasibility of the study including recruitment, enrollment, and retention rates 2 years. Throughout the course of the study (number recruited/screened, number enrolled, number completing the study)
Secondary Heart Rate Variability (HRV) Change in HRV from enrollment to post-treatment 12 weeks
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