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临床试验/NCT02552836
NCT02552836已完成不适用

Evaluation of Two Psychotherapies for Depressed Patients With Parkinson's Disease

Hopital Montfort2 个研究点 分布在 1 个国家目标入组 63 人开始时间: 2016年3月1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
63
试验地点
2
主要终点
Hamilton Depression Rating Scale (HAM-A)

研究概览

简要总结

The primary aim of this randomized controlled trial is to determine the acute antidepressant efficacy of interpersonal psychotherapy (IPT) in depressed patients with Parkinson's Disease.

详细描述

The primary aim of this study is to determine whether IPT is more efficacious than an intervention that controls for non-specific factors (i.e., supportive psychotherapy) in reducing depressive symptoms. A secondary aim is to determine whether IPT is better than supportive therapy in improving quality of life, interpersonal functioning, attachment patters, and motor symptoms, and whether treatment gains are durable at 6-months follow-up. An exploratory aim of the study is identify moderators and mediators of treatment outcome. Patients who meet study criteria will be randomly assigned to either 12 sessions of IPT or 12 sessions of supportive therapy. The primary efficacy measure (Hamilton Depression Rating Scale) will be administered at baseline, weeks 6 and 12, and at 6 months follow-up.

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 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Outpatients with idiopathic Parkinson's disease and between stages 1 and 3 in the modified Hohn & Yahr Clinical Staging Scale
  • •Diagnosis of a depressive disorder
  • •Score ≥ 12 on the 17-item Hamilton Depression Rating Scale
  • •Living independently

排除标准

  • •History of bipolar disorder or psychotic symptoms (other than drug induced)
  • •Substance-related disorders in the last 12 months
  • •Acutely suicidal or history of suicide attempts in the past 5 years
  • •Presence of cognitive deficits (i.e., score ≤ 24 on the Mini Mental Status Exam) or history of significant cognitive disorders
  • •Presence of other significant neurological problems
  • •Presence of unstable comorbid medical conditions
  • •Currently receiving psychotherapy
  • •Unable to attend weekly therapy sessions

研究组 & 干预措施

Interpersonal Psychotherapy (IPT)

Experimental

Patients assigned to IPT will receive 12 sessions of individual therapy of approximately 50 minutes duration. Therapy will be manualized and slightly adapted to meet the needs of patients with Parkinson's Disease. Therapy focuses on one of four interpersonal events that are linked with onset or maintenance of depression (role transition, role disputes, unresolved grief, and interpersonal deficits).

干预措施: Interpersonal Psychotherapy (Behavioral)

Supportive Psychotherapy (SP)

Active Comparator

Patients assigned to SP will receive 12 sessions of individual therapy of approximately 50 minutes duration. SP strives to create a supportive therapeutic relationship by emphasizing non-specific therapeutic interactions and techniques. Therapy will be manualized,

干预措施: Supportive Psychotherapy (Behavioral)

结局指标

主要结局

Hamilton Depression Rating Scale (HAM-A)

时间窗: Change from baseline to week 12 and 6-months follow-up

17-item clinician rated scale that assesses severity of depressive symptoms

次要结局

  • Beck Anxiety Inventory (BAI)(Change from baseline to week 12 and 6-months follow-up)
  • Experiences in Close Relationship Scale-Revised (ECR-R)(Change from baseline to week 12 and 6-months follow-up)
  • Parkinson's Disease Questionnaire (PDQ-39)(Change from baseline to week 12 and 6-months follow-up)
  • Interpersonal Relationships Inventory (IPRI)(Change from baseline to week 12 and 6-months follow-up)
  • Beck Depression Inventory (BDI)(Change from baseline to week 12 and 6-months follow-up)
  • Movement Disorders Society-Unified Parkinson's Disease Rating Scale (MDS-UPDRS)(Change from baseline to week 12 and 6-months follow-up)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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