Integration of a Behavioral Health Collaborative Care Model Into an ICU Recovery Clinic-Pilot for Families
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 150
- 试验地点
- 1
- 主要终点
- Consent Rate
研究概览
简要总结
This pilot study evaluates the feasibility and acceptability of implementing a Behavioral Health Collaborative Care Model (BH CoCM) for family members of ICU survivors. The intervention includes telehealth-enabled behavioral health assessments and access to the NeuroFlow platform. A subset of participants will undergo qualitative interviews.
详细描述
Patients seen in the MUSC ICU Recovery Clinic will be approached for consent for care through our Behavioral Health Collaborative Care Model. Patients and their families that consent will be randomized to an attention control group or an intervention group.
The intervention group will have access to NeuroFlow platform, which has been specifically designed to support delivery of a BH CoCM. They will utilize Neuroflow for 6 months. They will undergo assessments for anxiety, depression, post-traumatic stress The attention control group will undergo assessments for anxiety, depression, post-traumatic stress.
Investigators will look at changes over six months in intervention group compared to attention control group for patients in terms of symptoms of depression, anxiety, post-traumatic stress. Investigators will also look at adherence, BH CoCM implementation metrics, type and amount of guided content accessed in NeuroFlow. Investigators will perform qualitative surveys to understand better what patients thought about the intervention and ways in which it could be improved.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Supportive Care
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •- Family member of ICU Recovery Clinic patient enrolled in parent BH CoCM study
排除标准
- •Serious mental illness (e.g., schizophrenia, mania)
- •Late-stage dementia or cognitive impairment
- •Limited English proficiency
- •No internet-enabled device
- •Prisoners
研究组 & 干预措施
Control
Attention Control.
Interventional
干预措施: Behavioral Treatment (Behavioral)
结局指标
主要结局
Consent Rate
时间窗: Baseline
Investigators will assess the consent rate
Study Completion Rate
时间窗: enrollment to 6 months
We will assess the completion rate of all enrolled family members
次要结局
- Monthly Completion Rate of PHQ9 (Patient Health Questionnaire 9)(Enrollment to 6 months)
- Monthly Completion Rate of GAD 7 (General Anxiety Disorder 7)(baseline to 6 months)
- Monthly Completion Rate of PCL 5 (PTSD Checklist for DSM-5)(baseline to 6 months)
研究者
Rita Bakhru
Associate Professor-Faculty
Medical University of South Carolina