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临床试验/NCT04935060
NCT04935060已完成不适用

The Acceptability and Feasibility of a Guide for Sharing the Outcome of a Memory Assessment

University of Nottingham2 个研究点 分布在 1 个国家目标入组 7 人开始时间: 2021年9月21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
入组人数
7
试验地点
2
主要终点
Qualitative semi-structured interviews with clinicians.

研究概览

简要总结

The purpose of this study is to establish the acceptability of a guide developed to improve people's experiences of dementia assessment outcome appointments in comparison to a standard consultation. This study will also inform the feasibility of future research evaluating the guide and provide information on how well the measurements used provide evaluation of the intervention.

详细描述

Objectives:

To determine the acceptability of a guide supported consultation (intervention) for clinicians, patients and companions, in comparison to a standard diagnostic consultation (usual care).

To inform the feasibility of future research establishing recruitment processes and study uptake.

To establish how well the chosen measurement strategy provides evaluation of the intervention (including completion rates, perceived relevance and burdensomeness).

Setting:

研究设计

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

入排标准

年龄范围
65 Years 至 —(Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Patients will be included in the study if they are:
  • •Taking part in an initial assessment appointment with the participating MAS services
  • •Aged 18 years or over (Northamptonshire MAS require patients to be 65 years or over to be eligible for referral. There will be no upper age limit)
  • •Able to provide written informed consent
  • •Companions will be included in the study if they are:
  • •Supporting a patient-participant to attend a MAS initial assessment appointment
  • •Aged 18 years or over
  • •Able to provide written, informed consent
  • •MAS Clinicians will be included in the study if they are:
  • •Involved in the delivery of MAS outcome appointments
  • •Able to provide written informed consent

排除标准

  • •Patients and companions will not be included in the research if there is reason to doubt their capacity to give informed consent under the Mental Capacity Act
  • •Patients and companions who are not fluent in English will not be included in the study.

研究组 & 干预措施

Usual Care Dementia assessment

Active Comparator

Clinicians will conduct the assessment and outcome process as per their usual practice.

干预措施: Usual Care (Behavioral)

Guide informed dementia assessment

Experimental

The guide will be used by both clinicians, patients and their companions to inform the approach to the dementia assessment process.

干预措施: A guide to inform the process of delivering the outcomes of a dementia assessment (Behavioral)

结局指标

主要结局

Qualitative semi-structured interviews with clinicians.

时间窗: Interviews to take place within four weeks of clilnicians completing outcome appointments with all of the patients participating in the study.

Focussing on their experiences of using the guide and delivering outcome appointments.

Difference in scores on The Consultation and Relational Empathy (CARE) Questionnaire for each condition

时间窗: Post outcome appointment. Up to four weeks following outcome appointment.

Measures patient and companions rating of clinician empathy in consultations. Higher scores suggest higher levels of clinician empathy. The maximum score possible is 50 and the minimum is 10.

Qualitative semi-structured interviews with patients and companions.

时间窗: Interviews to take place following the outcome appointment. Up to four weeks following outcome appointment.

Focussing on their experiences of the outcome appointment.

Difference in scores on The Consultation and Relational Empathy (CARE) Questionnaire for each condition

时间窗: Baseline

Measures patient and companions rating of clinician empathy in consultations. Higher scores suggest higher levels of clinician empathy. The maximum score possible is 50 and the minimum is 10.

Difference in scores on The Consultation and Relational Empathy (CARE) Questionnaire for each condition

时间窗: Post initial Consultation. Up to four weeks following consultation appointment.

Measures patient and companions rating of clinician empathy in consultations. Higher scores suggest higher levels of clinician empathy. The maximum score possible is 50 and the minimum is 10.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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