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临床试验/NCT04610034
NCT04610034Unknown不适用

"Resilient Caregivers" - A Randomized Controlled Trial of a Resilience-based Intervention for Distressed Partner Caregivers of Cancer Patients

Danish Cancer Society1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2021年3月19日最近更新:
适应症

试验速览

阶段
不适用
入组人数
80
试验地点
1
主要终点
Change in symptoms of anxiety

研究概览

简要总结

The objective of this study is to develop and test the effectiveness of a resilience-based intervention for distressed partner caregivers of cancer patients in reducing symptoms of anxiety, depression and distress, while improving quality of life and resilience (meta-reflective skill, values clarification and coping strategies).

详细描述

Informal caregivers of cancer patients often experience significant psychological distress, which may even exceed that of the patient's. Partners or spouses are typically the most important caregiver and emotional support person for the cancer patient, but there is a lack of psychological interventions that specifically target caregiving partners. "Resilient Caregivers" is a novel 7-session group-based program aimed specifically at improving the participant's ability to cope with the stresses of being a partner to a cancer patient. In this randomized trial, the investigators aim to assess the potential efficacy of this program in improving the caregiver's resilience and quality of life, as well as reducing symptoms of anxiety, depression and distress. Outcomes will be assessed at baseline and at 3, 6 and 12-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
None

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

  • Partner/Spouse to a patient diagnosed with Stage I-III cancer and receiving cancer treatment at Herlev Hospital
  • Patient performance status 1 or 2
  • Distress Thermometer score > 4
  • Able to speak and understand Danish
  • Has given written informed consent to participate in the study

排除标准

  • Being a cancer patient
  • Has untreated psychopathology or physical impairment that may prevent attendance and participation in the study
  • Active substance abuse

结局指标

主要结局

Change in symptoms of anxiety

时间窗: Baseline, 3 months, 6 months and 12 months follow-up

Measured by Generalized Anxiety Disorder-7 (GAD-7); range 0-21; higher scores = more symptoms

次要结局

  • Change in perceived stress(Baseline, 3 months, 6 months and 12 months follow-up)
  • Change in symptoms of depression(Baseline, 3 months, 6 months and 12 months follow-up)
  • Change in valued living(Baseline, 3 months, 6 months and 12 months follow-up)
  • Change in resilience(Baseline, 3 months, 6 months and 12 months follow-up)
  • Change in rumination/worry and coping(Baseline, 3 months, 6 months and 12 months follow-up)
  • Change in psychological distress(Baseline, 3 months, 6 months and 12 months follow-up)
  • Change in sleep quality(Baseline, after completion of intervention (approximately 3 months from inclusion), 6 months and 12 months follow-up)
  • Change in quality of life(Baseline, 3 months, 6 months and 12 months follow-up)

研究者

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

Pernille Bidstrup

Principle investigator

Danish Cancer Society

研究点 (1)

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