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Clinical Trials/CTRI/2025/09/095401
CTRI/2025/09/095401
Not yet recruiting
Phase 3

Effect of Nurse-led program to improve self-efficacy in managing seizures among caregivers of children at tertiary care institute of Western Rajasthan

Gopal1 site in 1 country66 target enrollmentStarted: October 10, 2025Last updated:

Overview

Phase
Phase 3
Status
Not yet recruiting
Sponsor
Gopal
Enrollment
66
Locations
1
Primary Endpoint
Improvement in self-efficacy of caregivers in managing seizures, measured using the KidSIM-ASPIRE Parent Seizure Self-Efficacy Questionnaire (pre-test vs. post-test in experimental and control groups).

Overview

Brief Summary

This study aims to evaluate the effectiveness of a nurse-led program (simulation-based education and educational booklet) in improving self-efficacy among caregivers of children with seizures at a tertiary care institute in Western Rajasthan.

The primary hypothesis is that caregivers who undergo the nurse-led program will demonstrate a significant improvement in self-efficacy scores (measured by the KidSIM-ASPIRE Parent Seizure Self-Efficacy Questionnaire) compared to those receiving routine discharge instructions.

Secondary objectives include examining the association between caregivers’ demographic variables and their self-efficacy scores.

Study Design

Study Type
Interventional
Allocation
Other
Masking
None

Eligibility Criteria

Ages
1.00 Year(s) to 18.00 Year(s) (—)
Sex
All

Inclusion Criteria

  • Caregivers who are 1.Aged 18 to 60 years and are the primary caregiver of the child.
  • 2.Caring for children aged 1 to 18 years with seizures.
  • 3.Willing to participate and provide written informed consent.

Exclusion Criteria

  • Exclusion Criteria 1.Caregivers of children with other chronic co-morbid conditions.
  • 2.Caregivers with known psychiatric illnesses or cognitive impairments.

Outcomes

Primary Outcomes

Improvement in self-efficacy of caregivers in managing seizures, measured using the KidSIM-ASPIRE Parent Seizure Self-Efficacy Questionnaire (pre-test vs. post-test in experimental and control groups).

Time Frame: Baseline (Pre-test) | Before the intervention, both experimental and control groups will complete the KidSIM-ASPIRE Parent Seizure Self-Efficacy Questionnaire. | Intervention Phase | Experimental group: Receives nurse-led program (simulation-based education + booklet, ~40–45 minutes). | Control group: Receives routine discharge instructions. | Post-test | After 1 week of intervention, self-efficacy will be reassessed in both groups using the same tool.

Secondary Outcomes

  • Association between demographic variables and self-efficacy(Baseline (pre-test, before intervention))

Investigators

Sponsor
Gopal
Sponsor Class
Other []
Responsible Party
Principal Investigator
Principal Investigator

Gopal

AIIMS JODHPUR

Study Sites (1)

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