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临床试验/NCT04696484
NCT04696484已完成不适用

Feasibility of a Goal-based Agenda Setting Intervention for Informing Conversations in Adult Cystic Fibrosis Care

Dartmouth-Hitchcock Medical Center8 个研究点 分布在 1 个国家目标入组 219 人开始时间: 2021年1月14日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
219
试验地点
8
主要终点
Use of intervention responses with physician (patient-reported)

研究概览

简要总结

This study aims to assess the feasibility of a new, brief intervention, the 'coopeRATE Prompt', for informing conversations between patients and physicians in routine tele-health and in-person adult Cystic Fibrosis (CF) care. The coopeRATE Prompt is two questions designed to elicit patients' concerns and goals to facilitate collaborative goal setting within the health care visit. This is a prospective single arm study that will be conducted at four CF care centers in the United States.

详细描述

Participating patients will be asked to complete two online surveys. The first survey, which includes the coopeRATE Prompt intervention questions, is completed 1-4 days before their upcoming healthcare visit. After completing this survey and before their visit, patients' intervention responses are shared with their physician and, if requested, other members of their care team. The second patient survey is completed within 24 hours after their healthcare visit. Participating clinicians are asked to complete a single online survey within one month after completion of patient data collection.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Health Services Research
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

入选标准

  • have a diagnosis of CF
  • are 18 years of age or older
  • can read and write English
  • have a scheduled in-person or tele-health routine CF care visit
  • have access to internet and email

排除标准

  • does not have a diagnosis of CF
  • is less than 18 years of age
  • cannot read and write English
  • does not have a scheduled in-person or tele-health routine CF care visit
  • does have access to internet and email

结局指标

主要结局

Use of intervention responses with physician (patient-reported)

时间窗: Within 24 hours after completion of the healthcare visit

Patient-reported discussion of intervention responses (concerns and goals) in the visit with physician, assessed using two items with multiple choice (single answer) format. The first item assesses how many of the patient concerns were discussed and the second item assesses how many of the patient goals were discussed. Item response options are 'None of them', 'Some of them', or 'All of them'.

次要结局

  • Intervention completion (patient-reported)(1-4 days before the healthcare visit)
  • Satisfaction with time spent (patient-reported)(Within 24 hours after completion of the healthcare visit)
  • Preference for sharing intervention responses with other team members (patient-reported)(1-4 days before the healthcare visit)
  • Satisfaction with intervention timing (patient-reported)(Within 24 hours after completion of the healthcare visit)
  • Way(s) in which intervention was helpful (patient-reported)(Within 24 hours after completion of the healthcare visit)
  • Initiator of discussion (patient-reported)(Within 24 hours after completion of the healthcare visit)
  • Future receipt of intervention (patient-reported)(Within 24 hours after completion of the healthcare visit)
  • Impact on time spent with patients (clinician-reported)(Within 1 month following completion of patient data collection)
  • Intervention acceptability (patient-reported)(1-4 days before the healthcare visit)
  • Collaborative goal setting (patient-reported)(Within 24 hours after completion of the healthcare visit)
  • Shared decision-making (patient-reported)(Within 24 hours after completion of the healthcare visit)
  • Use of intervention responses with patients (clinician-reported)(Within 1 month following completion of patient data collection)
  • Reason(s) for not using intervention (sometimes used) (clinician-reported)(Within 1 month following completion of patient data collection)
  • Utility of intervention (patient-reported)(Within 24 hours after completion of the healthcare visit)
  • Use of intervention responses with other team members (patient-reported)(Within 24 hours after completion of the healthcare visit)
  • Preferred intervention timing (patient-reported)(Within 24 hours after completion of the healthcare visit)
  • Future use of intervention (clinician-reported)(Within 1 month following completion of patient data collection)
  • Frequency of intervention receipt (clinician-reported)(Within 1 month following completion of patient data collection)
  • Utility of intervention (clinician-reported)(Within 1 month following completion of patient data collection)
  • Way(s) in which intervention was helpful (clinician-reported)(Within 1 month following completion of patient data collection)
  • Reason(s) for not using intervention (never used) (clinician-reported)(Within 1 month following completion of patient data collection)
  • Intervention acceptability (clinician-reported)(Within 1 month following completion of patient data collection)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Glyn Jones-Elwyn

Professor

Dartmouth-Hitchcock Medical Center

研究点 (8)

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