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临床试验/NCT04618250
NCT04618250已完成不适用

A Cluster Randomized, Pilot Trial of Coordinated, Co-produced Care to Reduce Excess Mortality and Improve Quality of Life in Patients With Severe Mental Illness in General Practice Setting

University of Copenhagen1 个研究点 分布在 1 个国家目标入组 76 人开始时间: 2020年11月6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
76
试验地点
1
主要终点
Effectiveness of the collecting EQ5D-5L questionnaires

研究概览

简要总结

People with a severe mental illness (SMI) have an increased risk for premature mortality, predominantly due somatic health conditions. Evidence indicates that prevention and improved treatment of somatic conditions in patients with SMI could reduce this excess mortality. This paper reports a protocol designed to evaluate the feasibility and acceptability of a coordinated co-produced care programme (SOFIA model) in the general practice setting to reduce mortality and improve quality of life in patients with severe mental illness. The primary outcomes are description of study feasibility (recruitment and retention) and acceptability.

The SOFIA trial is designed as cluster randomized controlled trial targeting general practices in two regions in Denmark. 12 practices will each recruit 15 community-dwelling patients aged 18 and older with severe mental illness (SMI). Practices will be randomized in a ratio 2:1 to deliver a coordinated care program or care-as-usual during a 6 month period. An online randomized algorithm is used to perform randomization. The coordinated care program comprises enhanced educational training of general practitioners and their clinical staff, and prolonged consultations focusing on individual needs and preferences of the patient with SMI. Assessments are administered at baseline, and at end of study period.

If delivery of the intervention in the general practice setting proves feasible, a future definitive trial to determine the effectiveness of the intervention in reducing mortality and improving quality of life in patients with SMI can take place.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
Single (Outcomes Assessor)

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

  • Registered at a general practice situated in the Danish Capital Region or the Region of Zealand;
  • Registered at general practice with International Classification of Primary Care version 2 (ICPC-2) diagnostic code p72 (psychotic disorders);
  • Registered at general practice with ICPC-2 diagnostic code p73 (bipolar mood disorders);
  • Prescription of Lithium (Anatomical Therapeutic Chemical (ATC): N05AN);
  • Registered at general practice with ICPC-2 diagnostic code p76 AND (Prescription of Lamotrigine (N03A09) OR Carbamazepine (N03AF01) OR Valproic Acid (N03AG01));
  • Registered at general practice with ICPC-2 diagnostic code p76 (unipolar depressive disorders) AND (Prescription of tricyclic antidepressants (N06AA) AND/OR venlafaxine (N06AX16) AND/OR duloxetine (N06AX21) AND/OR Monoamine Oxidase A Inhibitor (MAOi) (N06AG) AND/OR non-selective MAOi (N06AF)).

排除标准

  • Subjected to any type of legal measure as stipulated in the Danish Mental Health Law;
  • Registered with a dementia diagnosis ICPC-2 p70 (dementia);
  • Receiving end-of-life care;
  • Non-Danish speakers;
  • Assumed by the patient's general practitioner to have an overall functional level that is too low for meaningful participation in trial.

结局指标

主要结局

Effectiveness of the collecting EQ5D-5L questionnaires

时间窗: 6 months after randomization

Proportion of returned and completed EQ5D-5L questionnaire.

Effectiveness of the design in terms of recruitment of practices and patients

时间窗: 6 months after randomization

Proportion of contacted general practices, which agree to participate in the study and the eligibility and consent rate of patients.

Acceptability of the intervention for patients and general practitioners, staff and patients.

时间窗: Entire study period (6 months)

Qualitative semi-structured interviews with patients and general practitioners, staff and patients.

Effectiveness of the collecting Multimorbidity Questionnaires

时间窗: 6 months after randomization

Proportion of returned and completed Multimorbidity Questionnaires.

Retention of patients during the study

时间窗: 6 months after randomization

Proportion of recruited patients in the intervention group who attend the first consultation.

Acceptability of REDcap software for general practitioners

时间窗: Entire study period (6 months)

Qualitative semi-structured interviews with general practitioners.

Mortality

时间窗: 6 months after randomization

Number of all-cause deaths of participants during the 6 month trial period.

Hospitalizations

时间窗: 6 months after randomization

Number of all-cause in- and outpatient hospitalizations of participants during the 6 months trial period.

次要结局

  • Multimorbidity Questionnaires (MMQ) scores(3 times during study period (at baseline, before prolonged consultation and 6 months after randomization)

研究者

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

Susanne Reventlow

Professor

University of Copenhagen

研究点 (1)

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