Intervention on Caregivers Caring for Patients Poststroke With Upper Limb Apraxia

Not Applicable

Completed

• Conditions: Emotional Stress; Performance Anxiety

• Registration Number: NCT02307019
• Lead Sponsor: Universidad de Granada

Brief Summary

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.

Detailed Description

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.

Study Timeline

• Study Start: 2014-07
• Study First Submitted: 2014-12-01
• Study First Submitted QC: 2014-12-01
• Study First Posted: 2014-12-03
• Primary Completion: 2018-09
• Study Completion: 2018-09
• Status Verified: 2018-10
• Last Update Submitted: 2018-10-04
• Last Update Posted: 2018-10-05

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 50

Inclusion Criteria

• 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.

Exclusion Criteria

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

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Change from Baseline in Stroke Impact Scale (SIS-16) at 16 weeks	Sixteen weeks
Change from Baseline in Stroke Impact Scale (SIS-16) at 8 weeks	Eight weeks

Secondary Outcome Measures

Name	Time	Method
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 General health questionnaire (GHQ-28) at 16 weeks	Sixteen weeks
Change from Baseline in Zarit questionnaire at 16 weeks	Sixteen weeks
Change from Baseline in Disabilities of the Arm, Shoulder and Hand (Quick-DASH) at 16 weeks	Sixteen weeks

Trial Locations

Locations (1)

University of Granada; 🇪🇸 Granada, Andalucía, Spain