Feasibility Pilot Trial of a Pharmacist-led Medication Management Intervention for Multi-Morbid Adults With Chronic Obstructive Pulmonary Disease
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 入组人数
- 92
- 主要终点
- Proportion of eligible patients recruited to the intervention
研究概览
简要总结
A pilot trial to examine feasibility of a pharmacist-led intervention for patients with COPD (Chronic Obstructive Pulmonary Disease) and multimorbidity to improve medication safety and reduce dyspnea. Patients will receive inhaler teaching and medication optimization counseling. Outcomes include feasibility, acceptability, appropriateness, and exploratory measures such as medication discontinuation and patient-reported symptom burden.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 45 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Diagnosis of COPD
- •Medicare/Medicaid insured
- •Using an inhaler
- •Reports dyspnea or suboptimal medication adherence
排除标准
- •Under age 18 (caregivers/clinicians)
- •Under age 45 (patients)
- •Opioid use disorder
- •Cognitive impairment
- •Unable to communicate in English
研究组 & 干预措施
Pharmacist-led Medication Management
Pharmacist visit for inhaler teaching and medication optimization with follow-up at weeks 4 and 12.
干预措施: Pharmacist-led Medication Management Intervention (Behavioral)
结局指标
主要结局
Proportion of eligible patients recruited to the intervention
时间窗: Through the end of enrollment period, up to approximately 1 year
A measure of feasibility of the intervention.
次要结局
- Acceptability of Intervention Measure (AIM)(Baseline, 4 weeks, 12 weeks)
- Feasibility of Intervention Measure (FIM)(Baseline, 4 weeks, 12 weeks)
- Intervention Appropriateness Measure (IAM)(Baseline, 4 weeks, 12 weeks)
- Modified Medical Research Council (mMRC) questionnaire to measure dyspnea(Baseline, 4 weeks, 12 weeks)
- Medication side effect burden, measured via Living with Medicines Questionnaire (LMQ-3)(Baseline, 4 weeks, 12 weeks)
- Shared Decision Making (SDM-Q-9) questionnaires(Baseline, 4 weeks, 12 weeks)