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Feasibility & Acceptability of a Virtual Sister Circle Intervention for Black Women With Depressive Symptoms

NCT04837573 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2023-10-19

No results posted yet for this study

Summary

The purpose of this study is to evaluate the feasibility and acceptability of a protocol for middle- and older-aged Black women with depressive symptoms.

Conditions

Interventions

BEHAVIORAL

Sister Circle protocol

The intervention is an 8-week, therapeutically-informed protocol.

Sponsors & Collaborators

  • Kia Skrine Jeffers, PhD, RN, PHN

    lead OTHER

Principal Investigators

  • Kia Skrine Jeffers, PhD, RN, PHN · University of California, Los Angeles

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
40 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2022-09-14
Primary Completion
2023-04-02
Completion
2023-04-02

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04837573 on ClinicalTrials.gov