Increasing Uptake of Behavioral Weight Loss Programs Among Primary Care Patients
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 66
- 试验地点
- 1
- 主要终点
- Number of Participants Attending 6 Month Follow-up Appointment
研究概览
简要总结
This pilot trial will test feasibility and acceptability of a primary care-based intervention that aims to increase the portion of patients who enter evidence-based behavioral weight loss treatment.
详细描述
This trial is a pilot, pragmatic cluster randomized trial conducted in primary care clinics to determine intervention acceptability and the feasibility of proposed study protocol.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Other
- 盲法
- Single (Outcomes Assessor)
盲法说明
Staff recruiting participants and doing outcomes assessment will remain blinded to treatment assignment
入排标准
- 年龄范围
- 18 Years 至 75 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Primary care provider Inclusion criteria:
- •Employed by Duke PCRC clinic as primary care provider at least ½ FTE.
- •Has a primary adult panel
- •Has worked at Duke PCRC clinic for at least one year
- •Patient inclusion criteria
- •BMI ≥ 30 kg/m2 as measured at any clinic in previous 12 months.
- •English speaking
- •Self-report BMI ≥ 29 kg/m2 (to allow for under-reporting)
- •Regular email usage, defined as accessing email 3 or more times per week (on home or work computer or cell phone)
- •Age 18-75
- •Clinical appointment (well visit or chronic care visit) with enrolled Duke provider in 2-6 weeks of record review.
- •At least one prior appointment with the provider they are scheduled to see at target clinical appt.
- •Has a valid email address in electronic health records.
排除标准
- •In weight loss treatment program in past year
- •Unable to read content on websites without any assistance
研究组 & 干预措施
Intervention arm
Participant receives intervention to motivate weight loss treatment initiation and access to weight loss treatment.
干预措施: Motivational Intervention (Behavioral)
Comparator Arm
Participant receives access to weight loss treatment alone.
干预措施: Comparator Intervention (Other)
结局指标
主要结局
Number of Participants Attending 6 Month Follow-up Appointment
时间窗: 6 months
Count of enrolled participants who attend 6 month follow-up appointment
次要结局
- Intervention Acceptability (Acceptability Outcome)(1 month)