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临床试验/NCT04837573
NCT04837573已完成不适用

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

Kia Skrine Jeffers, PhD, RN, PHN2 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2022年9月14日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
30
试验地点
2
主要终点
Assess Acceptability according to the Theoretical Framework of Acceptability

研究概览

简要总结

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.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
40 Years 至 —(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Identify as Black or African American
  • 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

排除标准

  • Have a diagnosis of bipolar, but is not taking medication for the condition
  • Experiencing psychosis

研究组 & 干预措施

Group 1 Intervention, Weeks 1-8

Experimental

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

干预措施: Sister Circle protocol (Behavioral)

Group 2 Intervention, Weeks 9-16

Active Comparator

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

干预措施: Sister Circle protocol (Behavioral)

结局指标

主要结局

Assess Acceptability according to the Theoretical Framework of Acceptability

时间窗: 16 weeks

Qualitative assessment of Acceptability. The interview guide will be organized according to the constructs of the Theoretical Framework of Acceptability. Methodological conventions of qualitative description will be used to analyze the data.

Recruitment, completion, and retention rates of participants

时间窗: 16 weeks

80 percent recruitment, 80 percent completion, and 75 percent retention

次要结局

  • Changes in Acceptance and Action Questionnaire II (AAQ-II) from baseline at 8 weeks and 16 weeks(baseline, 8 weeks, 16 weeks)
  • Changes in Positive and Negative Affect Schedule (PANAS) Scale from baseline at 8 weeks and 16 weeks(baseline, 8 weeks, 16 weeks)
  • Changes in Perceived Stress Scale (PSS) from baseline at 8 weeks and 16 weeks(baseline, 8 weeks, 16 weeks)

研究者

发起方
Kia Skrine Jeffers, PhD, RN, PHN
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Kia Skrine Jeffers, PhD, RN, PHN

Assistant Professor

University of California, Los Angeles

研究点 (2)

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