跳至主要内容
临床试验/NCT05335382
NCT05335382进行中(未招募)不适用

Implementation and Evaluation of Primary Care Behavioral Health in Sweden - A Cluster Randomized Design for Superiority and Non-superiority Comparisons of Effects on Patient Reach, Availability, Costs, Sick-leave, Model Fidelity, and Patients' Everyday Function, Symptoms, and Experiences

Linnaeus University21 个研究点 分布在 1 个国家目标入组 666 人开始时间: 2022年1月1日最近更新:
适应症

试验速览

阶段
不适用
状态
进行中(未招募)
发起方
入组人数
666
试验地点
21
主要终点
WHO Disability Assessment Schedule 2.0 12-item (WHODAS-12) (4 domains)

研究概览

简要总结

In this multicenter study, the investigators want to compare treatment outcomes for patients with mental and behavioral health problems in traditional primary care (Care As Usual, CAU) and primary care centres that work according to the Primary Care Behavioral Health (PCBH) model. In addition to this, the investigators want to study organisation-level outcomes, such as access to care, perceived teamwork and work environment. To achieve this, primary care centres that have expressed interest in implementing PCBH will be cluster randomised between implementing directly or waiting for implementation.

详细描述

The overarching goal of primary care is to offer all patients individualised and context-sensitive healthcare with high access and continuity. One of the reasons primary care struggles with this goal is that a large proportion of patients suffer from mental and behavioural health problems, alone or in combination with one or several chronic illnesses. Despite many patients needing psychosocial interventions, there is a lack of mental health professionals as well as clear pathways for these patients.

Primary Care Behavioral Health (PCBH) is an innovative way of organising primary care, where mental health professionals have more yet shorter visits, strive for same-day access, and have an active consulting role in the primary care team. To help patients achieve relevant behavioral changes, so called brief interventions are used, which are based on isolated components from psychological treatments such as Cognitive Behavioral Therapy (CBT) and Acceptance and Commitment Therapy (ACT). Brief interventions usually stretch over 1-4 treatment sessions. Assessments within the model are generally contextual and largely avoid psychiatric diagnostics, instead focusing on the patient's situation and their associated coping strategies - whether they be positive or negative. Although PCBH is gaining in popularity, recent reviews conclude that among the evaluation trials there are very few comparative studies. As such, there is a great need for proper evaluation of a method that is already widely implemented.

Data will be collected at 17 primary care centers (PCCs) in Västra Götalandsregionen, Sweden, that have expressed an interest in implementing PCBH. The study is looking at both patient and organizational level variables. The PCCs will be randomized between implementing PCBH immediately (December 2021) or delayed with 5-9 months (implementation in late spring or early autumn of 2022). Outcome data will be collected also from the PCCs waiting for implementation, while they apply Care as Usual (CAU). Collection of patient self-ratings will start before the first implementation of PCBH to ensure functional data collection routines and possibly create a longer baseline, but the main analysis will use data from the period from when PCCs in the Early implementation arm actually have implemented PCBH to a good enough level and until PCCs in the control group start their implementation. Data from all PCCs will be continuously be collected also during the period when the delayed group implements PCBH. For individual patients, the primary end-point for the primary outcome (everyday functioning) will be 12 weeks after the first visit. Patient outcomes are also measured after 1 year.

Outcome at the organizational level will be measured in several ways, and here the primary outcome will be two measures of waiting time between identification of patient (i.e. them self-referring for mental or behavioral health issues) and the first visit: (a) actual waiting-time and (b) Outcome at the organizational level will be measured in several ways, and here the primary outcome will be two measures of waiting time between identification of patient (i.e. them self-referring for mental or behavioral health issues) and the first visit: (a) actual waiting-time for each patient identified as relevant for inclusion and (b) Third Next Available Appointment (TNAA) for the PCC as a whole, measured at the same day and time each week.

Fidelity will be measured by an expert group as well as using four questionnaires, one for each of mental health professionals, medical doctors, registered nurses and leadership. Implementation data will also be collected from these professional groups/roles at the implementing PCCs, for example with the s-NoMAD questionnaire.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Outcomes Assessor)

盲法说明

Patients will only be informed that the study is assessing the quality of primary care, and will not know that PCBH has been or will be implemented. Since primary and most secondary outcomes are patient-rated, outcomes assessors are also deemed to be blind.

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

  • All patients from age 18 who seek care at the PCC, who are deemed to be suitable for Behavioural Health interventions and booked to the mental health professionals at the PCC, according to screening methods and/or clinical assessments made by health care personnel at the PCC, will be included. This broad criteria reflects the naturalistic setting where decisions of clinicians, rather than highly standardized criteria, are the basis for inclusion.

排除标准

  • Does not speak Swedish well enough to fill out questionnaires.
  • Is in need of emergency type care, like with suicidal ideation or behaviours, ongoing psychosis or mania.

结局指标

主要结局

WHO Disability Assessment Schedule 2.0 12-item (WHODAS-12) (4 domains)

时间窗: Change during the period Pre, Week 4, Week 8, and Week 12

The eight items constituting the four domains of Life activities, Cognition, Getting along, and Participation in the 12-item version of the WHO Disability Assessment Schedule 2.0 (WHODAS-12) will be used as primary outcome, since these are condition-independent measures of Behavioral Health relevant everyday functioning. The scale ranges from 0 to 32 points. A lower score means better functioning. As such, a lower score is a better outcome.

Waiting time until first appointment

时间窗: From documented identification/self-referral to documented first visit at PCC (up to 6 months after identification)

Waiting time from the patient contacting their PCC with a behavioural health concern to being seen by a physician or psychosocial resource among patients in the study

次要结局

  • Third next available appointment (TNAA)(Measured each week from implementation to up to 2 years)
  • Generalized Anxiety Disorder 2-item (GAD-2)(Change during the period Pre, Week 4, Week 8, Week 12 and 1 year)
  • Short Health Anxiety Inventory 3-item (SHAI-MINI-3)(Change during the period Pre, Week 4, Week 8, Week 12 and 1 year)
  • Description of Behavioral Health Plan (PCBH) as structured note by clinician in medical record(Week 12)
  • Generalized Anxiety Disorder 7-item (GAD-7)(Change during the period Pre, Week 12 and 1 year)
  • Insomnia Severity Index 2-item (ISI-MINI-2)(Change during the period Pre, Week 4, Week 8, Week 12 and 1 year)
  • Patient-rated perception and attitude toward care provider(Week 12)
  • Patient recollection of plan/goal/methods, descriptions of behaviour changes made(Week 12)
  • Long-term WHO Disability Assessment Schedule 2.0 12-item (WHODAS-12) (4 domains)(Change during the period Pre, Week 4, Week 8, Week 12, and 1 year)
  • WHO Disability Assessment Schedule 2.0 12-item (WHODAS-12) (2 domains)(Change during the period Pre, Week 12 and 1 year)
  • Social Phobia Inventory - Abbreviated version (Mini-SPIN)(Change during the period Pre, Week 4, Week 8, Week 12 and 1 year)
  • The Alcohol Use Disorders Identification Test-Concise (AUDIT-C)(Change during the period Pre, Week 4, Week 8, Week 12 and 1 year)
  • Pain One-item Rating(Change during the period Pre, Week 4, Week 8, Week 12 and 1 year)
  • Total symptom index(Change during the period Pre, Week 4, Week 8, Week 12 and 1 year)
  • Brunnsviken Brief Quality of Life Questionnaire (BBQ)(Change during the period Pre, Week 12 and 1 year)
  • Adverse Events-3(Week 4, Week 8)
  • Patient Health Questionnaire 9-Item (PHQ-9)(Change during the period Pre, Week 12 and 1 year)
  • Patient Health Questionnaire 2-Item (PHQ-2)(Change during the period Pre, Week 4, Week 8, Week 12 and 1 year)
  • Panic Disorder Severity Scale - Self rated 2-item (PDSS-SR-MINI-2)(Change during the period Pre, Week 4, Week 8, Week 12 and 1 year)
  • Perceived Stress Scale (PSS-MINI-2) + 2 new questions(Change during the period Pre, Week 4, Week 8, Week 12 and 1 year)
  • Outcome Rating Scale (ORS)(Change during the period Pre, Week 4, Week 8, Week 12 and 1 year)
  • Session Rating Scale (SRS)(Change during the period Pre, Week 4, Week 8, Week 12 and 1 year)
  • Experienced negative/Adverse Events, where the worst and most probably care-induced event is more thoroughly described and rated on severity and perceived cause(Week 12)
  • Karolinska Exhaustion Disorder Scale 3-item (KEDS-3) + 2 confirming questions from the Swedish questionnaire 'självskattat utmattningssyndrom' (s-UMS) ['self-rated burnout-syndrome'](Change during the period Pre, Week 4, Week 8, Week 12 and 1 year)
  • Obsessive Compulsive Disorder 3-Item (OCD-3-MINI)(Change during the period Pre, Week 4, Week 8, Week 12 and 1 year)
  • Adverse Events-9(Week 12)
  • Well-being Behaviors(Change during the period Pre, Week 12 and 1 year)

研究者

发起方
Linnaeus University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Viktor Kaldo

Professor

Linnaeus University

研究点 (21)

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