Skip to content

Effectiveness of a Home-based Ergonomic Intervention Program in Caregivers of Chronic Post-stroke Patients

Effectiveness of a Home-based Ergonomic Intervention Program on Overall Quality of Life, Health Satisfaction, and Home Ergonomics in Caregivers of Chronic Post-stroke Patients: a Randomized Controlled Clinical Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03284580
Enrollment
33
Registered
2017-09-15
Start date
2017-01-08
Completion date
2017-08-20
Last updated
2017-09-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Quality of Life, Stroke

Brief summary

The objective of the present study is to evaluate the effectiveness of two home-based ergonomic intervention programs compared to a control group on the quality of life of caregivers of post-stroke patients

Detailed description

Stroke is a neurological pathology that can cause functional problems and an impairment to perform activities of daily living at home. For this reason, these patients need the support of a caregiver. Caregivers of post-stroke patients often have also problems with their quality of life because of the care that they must provide. These problems appear mainly during the support tasks in the activities performed at the patient's home. The objective of the present study is to evaluate the effectiveness of two home-based ergonomic intervention programs compared to a control group on the quality of life of caregivers of post-stroke patients

Interventions

An ergonomic intervention program focused to caregivers, including recommendation about how they should help themself and the patients activities at home.

OTHERPostural plus kinesiotherapy intervention program

An ergonomic intervention program focused to caregivers, including recommendation about how they should help themself and the patients activities at home.

OTHERControl or conservative intervention

A control or conservative intervention, including general information about stroke disease for the caregivers of these patients

Sponsors

Universidad de Granada
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Being caregivers of post-stroke patients * Being over 18 years old

Exclusion criteria

* Being caregiver of patients with other neurological patients

Design outcomes

Primary

MeasureTime frameDescription
Change from WhoQol-Bref at 8 weeksEight weeksThis test measures quality of life
Change from WhoQol-Bref at 16 weeksSixteen weeksThis test measures quality of life

Secondary

MeasureTime frameDescription
Change from ergonomic evaluation of the domestic environment at 8 weeksEight weeksThis measurement evaluates if domestic environment is ergonomic
Change from ergonomic evaluation of the domestic environment at 16 weeksSixteen weeksThis measurement evaluates if domestic environment is ergonomic

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 7, 2026