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Association between strain on informal caregiver and quality of life of stroke patient

Correlation between strain on informal caregiver and quality of life of stroke patient - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CTRI
Registry ID
CTRI/2024/03/063660
Enrollment
44
Registered
2024-03-06
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-01

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

Conditions

Health Condition 1: G811- Spastic hemiplegia

Interventions

Control Intervention1: NIL: NIL

Sponsors

Subrat Tripathi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 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

Exclusion criteria

Exclusion criteria: 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.).

Design outcomes

Primary

MeasureTime frame
Zarit caregiver burden assessment. 5 dimensions of SF-36Timepoint: 1 time

Secondary

MeasureTime frame
Stroke specific quality of life (SSQOL)Timepoint: 1 time

Countries

India

Contacts

Public ContactDr Neha Gupta

Amity Institute of health allied sciences

ngupta4@amity.edu9810280418

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026