CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 30 enrolled / 30 target
Drug / intervention
Sister Circle protocolbehavioral
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT04837573
NCT04837573N/ACompletedOn Track (0.7/mo)Completion was 39mo ago
CompareCT.gov

Evaluating the Feasibility and Acceptability of a Therapeutically-Grounded Virtual Sister Circle Intervention for Black Women With Depressive Symptoms

Kia Skrine Jeffers, PhD, RN, PHN·interventional·Posted Apr 8, 2021·Updated Jun 5, 2026

In Brief

A clinical study evaluating Sister Circle protocol for Depressive Symptoms and Depression. Completed, enrolled 30 participants across 1 site.

Detailed 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.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsDepressive Symptoms, Depression
CountriesUnited States
CollaboratorsNational Institute on Aging (NIA), National Center for Advancing Translational Sciences (NCATS)

Timeline

N/ACompletedFinished
20222023202420252026
First PostedApr 8, 2021
Enrollment StartSep 14, 2022
Primary CompletionApr 2, 2023
TodayJul 2, 2026
Enrollment to primary: 7 monthsPosted 5.2 years ago

Arms & Interventions

Group 1 Intervention, Weeks 1-8experimental

During Weeks 1-8, Group 1 receives the Intervention and Group 2 receives no treatment.

Behavioral: Sister Circle protocol
Group 2 Intervention, Weeks 9-16active_comparator

During Weeks 9-16, Group 2 receives the Intervention and Group 1 receives no treatment.

Behavioral: Sister Circle protocol

Interventions

Sister Circle protocolbehavioral

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