Association between strain on informal caregiver and quality of life of stroke patient
- Conditions
- Health Condition 1: G811- Spastic hemiplegia
- Registration Number
- CTRI/2024/03/063660
- Lead Sponsor
- Subrat Tripathi
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
1) Stroke Survivor: Participants must be individuals who have been diagnosed with a stroke.
2) Family Involvement: Participants should have family members(e.g., spouses, children, caregivers) actively involved in their care.
3) Consent: Participants or their legal representatives must provide informed consent to participate in the study.
4) Health Status: Participants should be stable in terms of their medical condition at the time of enrollment to minimize confounding variables.
5) 6 Months of stroke
6) Care taker must be in good health
7) Both caregivers and stroke patients should be willing and able to participate in the study
1) Other Significant Medical Conditions: Individuals with severe, uncontrolled comorbid medical conditions apart from stroke may be excluded.
2) Cognitive Impairment: Participants with severe cognitive impairments that prevent them from engaging in the activity.
3) Language Barrier: Those who do not have sufficient language skills to understand the educational materials may be excluded.
4) Lack of Family Involvement: If there is no active family involvement in the care of the stroke survivor, these individuals
might be excluded.
5) Unwillingness to Participate: Individuals who decline to provide informed consent or actively refuse participation are typically excluded.
6) Other Research Participation: Participants currently involved in other conflicting research studies may be excluded to avoid data contamination.
7) Caregivers with severe psychological or physical health conditions that may interfere with their ability to participate.
8) Patients or caregivers who have experienced recent major life events that could significantly impact their quality of life or caregiving burden (e.g., recent bereavement, divorce, etc.).
Study & Design
- Study Type
- Observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Zarit caregiver burden assessment. <br/ ><br>5 dimensions of SF-36Timepoint: 1 time
- Secondary Outcome Measures
Name Time Method Stroke specific quality of life (SSQOL)Timepoint: 1 time