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临床试验/NCT04613076
NCT04613076已完成不适用

A Collaborative, Computer-assisted, Psycho-educational Intervention for Depressed Patients With Chronic Disease at Primary Care

University of Chile1 个研究点 分布在 1 个国家目标入组 359 人开始时间: 2019年9月3日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
359
试验地点
1
主要终点
Depression change

研究概览

简要总结

Background: depression and chronic diseases are frequently comorbid public health problems. However, clinical guidelines often fail to consider comorbidities. This study protocol describes a cluster randomized trial (CRT) aimed to compare the effectiveness of a collaborative, computer-assisted, psycho-educational intervention versus enhanced usual care (EUC) in the treatment of depressed patients with hypertension and/or diabetes in primary care clinics (PCC) in Santiago, Chile.

Methods: two-arm, single-blind, CRT carried out at two municipalities in Santiago, Chile. Eight PCC will be randomly assigned (1:1 ratio within each municipality, 4 PCC in each municipality) to the INTERVENTION or EUC. A total of 360 depressed patients, aged at least 18 years, with Patient Health Questionnaire-9 Item [PHQ-9] scores ≥ 15, and enrolled in the Cardiovascular Health Program at the participating PCC. Patients with alcohol/substance abuse; current treatment for depression, bipolar disorder, or psychosis; illiteracy; severe impairment; and resident in long-term care facilities, will be excluded. Patients in both arms will be invited to use the Web page of the project, which includes basic health education information. Patients in the INTERVENTION will receive eight sessions of a computer-assisted, psycho-educational intervention delivered by trained therapists, a structured telephone calls to monitor progress, and usual medical care for chronic diseases. Therapists will receive biweekly and monthly supervision by psychologist and psychiatrist, respectively. A monthly meeting will be held between the PCC team and a member of the research team to ensure continuity of care. Patients in EUC will receive depression treatment according to clinical guidelines and usual medical care for chronic diseases. Outcome assessments will be conducted at three, six, and twelve months after enrollment. The primary outcome will be depression improvement at six months, defined as ≥ 50% reduction in baseline PHQ-9 scores. Intention-to-treat analyses will be performed.

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
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

  • Age 18 or older.
  • Enrolled in the Cardiovascular Health Program (i.e. currently receiving treatment for diabetes and/or hypertension) at the study primary care clinics.
  • Patient Health Questionnaire-9 Item (PHQ-9) score ≥
  • Signed informed consent.

排除标准

  • Functional illiteracy (i.e., patients unable to read and comprehend written information, such as the study questionnaires or written informed consent).
  • Significant visual and/or auditive impairments (i.e., such as those imposing a serious difficulty to respond the study questionnaires or written informed consent).
  • Pregnancy or breastfeeding.
  • Cognitive impairment - ineligible patients would give a negative answer to questions "What year is it?" and "Where are we (place/address)?".
  • In treatment for bipolar and/or psychotic disorder.
  • Current psychological treatment for depression.
  • High risk of developing alcohol/substance abuse problems, according to an Alcohol, Smoking and Substance Involvement Screening Test (ASSIST) score ≥ 27.

结局指标

主要结局

Depression change

时间窗: Even though the primary outcome is taken at six-month follow-up, this measure will also be reported at three- and twelve-month follow-up.

Defined as a 50% reduction in a participant's Patient Health Questionnaire-9 Item (PHQ-9) score compared to the baseline. The PHQ-9 minimum and maximum values are 0 and 27 points. Higher scores mean worse outcomes.

次要结局

  • Health-related quality of life(Three-, six-, and twelve-month follow-up.)
  • Ad-hoc questionnaire for the assessment of the acceptability of depression treatment(Three-, six-, and twelve-month follow-up.)
  • Proportion of patients who change their depressive status(Three-, six-, and twelve-month follow-up.)
  • Proportion of participants with change in blood pressure(Three-, six-, and twelve-month follow-up.)
  • Social solving problem skills(Three-, six-, and twelve-month follow-up.)
  • Proportion of participants with change in glycosylated hemoglobin(Three-, six-, and twelve-month follow-up.)

研究者

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

Graciela Rojas Castillo

Professor

University of Chile

研究点 (1)

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