Feasibility & Acceptability of a Virtual Sister Circle Intervention for Black Women With Depressive Symptoms
NCT ID: NCT04837573
Last Updated: 2023-10-19
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
30 participants
INTERVENTIONAL
2022-09-14
2023-04-02
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NON_RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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Group 1 Intervention, Weeks 1-8
During Weeks 1-8, Group 1 receives the Intervention and Group 2 receives no treatment.
Sister Circle protocol
The intervention is an 8-week, therapeutically-informed protocol.
Group 2 Intervention, Weeks 9-16
During Weeks 9-16, Group 2 receives the Intervention and Group 1 receives no treatment.
Sister Circle protocol
The intervention is an 8-week, therapeutically-informed protocol.
Interventions
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Sister Circle protocol
The intervention is an 8-week, therapeutically-informed protocol.
Eligibility Criteria
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Inclusion Criteria
* Identify as female
* Age 40 years and older
* Community-dwelling
* Self-report of experiencing depressive symptoms
* Ability to commit to the 8-week intervention
* Access to Zoom
* Speak and read English
Exclusion Criteria
* Experiencing psychosis
40 Years
FEMALE
No
Sponsors
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Kia Skrine Jeffers, PhD, RN, PHN
OTHER
Responsible Party
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Kia Skrine Jeffers, PhD, RN, PHN
Assistant Professor
Principal Investigators
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Kia Skrine Jeffers, PhD, RN, PHN
Role: PRINCIPAL_INVESTIGATOR
University of California, Los Angeles
Locations
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University of California, Los Angeles
Los Angeles, California, United States
Countries
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Other Identifiers
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21-002949
Identifier Type: -
Identifier Source: org_study_id
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