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临床试验/CTRI/2025/09/095401
CTRI/2025/09/095401尚未招募3 期

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

Gopal1 个研究点 分布在 1 个国家目标入组 66 人开始时间: 2025年10月10日最近更新:

试验速览

阶段
3 期
状态
尚未招募
发起方
入组人数
66
试验地点
1
主要终点
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).

研究概览

简要总结

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.

研究设计

研究类型
Interventional
分配方式
Other
盲法
None

入排标准

年龄范围
1.00 Year(s) 至 18.00 Year(s)(—)
性别
All

入选标准

  • 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.

排除标准

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

结局指标

主要结局

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).

时间窗: 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.

次要结局

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

研究者

发起方
Gopal
申办方类型
Other []
责任方
Principal Investigator
主要研究者

Gopal

AIIMS JODHPUR

研究点 (1)

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