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临床试验/NCT02307019
NCT02307019已完成不适用

Intervention on Caregivers Caring for Patients Poststroke With Upper Limb Apraxia: Randomized Clinical Trial

Universidad de Granada1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2014年7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
50
试验地点
1
主要终点
Change from Baseline in Stroke Impact Scale (SIS-16) at 8 weeks

研究概览

简要总结

The purpose of this study is to analyze the effects of a intervention on a specific health prevention/intervention program aimed at caregivers of mild and moderate patients post stroke with upper limb apraxia in comparison to a control group with a no specific formation in that kind of patients.

详细描述

Patients with Upper limb apraxia after stroke have severe problems to adapt their daily life.

The upper limb apraxia syndrome affects the performance of skilled movements carried out by the upper limbs and provoke that many patients´activities have to be made by their main caregiver or carers.

Caregivers usually have to occupy much time and efforts for caring their familiar or client, and it can result in a overload in different areas of the caregiver health.

Few data are available on the effectiveness of interventions in caregivers that informally works with that kind of patients.

The specific prevention health program is based on improving the awareness of the assistance that the caregivers provide, and knowing the process of the information that carer has to give to the patient while the patients have their activities made.

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 (Care Provider, Investigator)

入排标准

年龄范围
18 Years 至 90 Years(Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Having an habitual role of carer (informal or formal).
  • •Being caring a mild-moderate poststroke patient with upper limb apraxia.
  • •Subjective manifestations of overload in the role as carer.
  • •More than two month as carer.

排除标准

  • •Uncooperativeness
  • •Being formed in the care of that kind of patients

研究组 & 干预措施

Program on specific prevention of health

Experimental

The caregivers will be randomly assigned to an experimental group, to receive the program on specific prevention of health. The workshop will be performed twice a month, two hours a day, during a 4-week period.

干预措施: Program on specific prevention of health (Other)

Program on general prevention of health

Active Comparator

Control group will receive an intervention by mean of a general health program to manage the common situations when a caregiver is caring for a patient with dependency. The workshop will be performed two a month, two hours a day, during a 4-week period.

干预措施: Program on general prevention of health (Other)

结局指标

主要结局

Change from Baseline in Stroke Impact Scale (SIS-16) at 8 weeks

时间窗: Eight weeks

Change from Baseline in Stroke Impact Scale (SIS-16) at 16 weeks

时间窗: Sixteen weeks

次要结局

  • Change from Baseline in Barthel index at 8 weeks(Eight weeks)
  • Change from Baseline in Disabilities of the Arm, Shoulder and Hand (Quick-DASH) at 8 weeks(Eight weeks)
  • Change from Baseline in Barthel index at 16 weeks(Sixteen weeks)
  • Change from Baseline in family APGAR at 16 weeks(sixteen weeks)
  • Change from Baseline in Duke-UNC-11 questionnaire of functional social support at 8 weeks(Eight weeks)
  • Change from Baseline in Duke-UNC-11 questionnaire of functional social support at 16 weeks(Sixteen weeks)
  • Change from Baseline in General health questionnaire (GHQ-28) at 8 weeks(Eight weeks)
  • Change from Baseline in family APGAR at 8 weeks(Eight weeks)
  • Change from Baseline in Zarit questionnaire at 8 weeks(Eight weeks)
  • Change from Baseline in Disabilities of the Arm, Shoulder and Hand (Quick-DASH) at 16 weeks(Sixteen weeks)
  • Change from Baseline in General health questionnaire (GHQ-28) at 16 weeks(Sixteen weeks)
  • Change from Baseline in Zarit questionnaire at 16 weeks(Sixteen weeks)

研究者

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

Encarnación Aguilar Ferrandiz

Intervention on caregivers caring for patients poststroke with upper limb apraxia: Randomized Clinical Trial

Universidad de Granada

研究点 (1)

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