comparison between knowledge of caregivers of children with acute leukemia recieving video based education regarding prevention of infection during chemotherapy and the ones recieving routine care

A randomized control trial to evaluate the effect of video based education on knowledge of caregivers of children with acute leukemia regarding prevention of infection during chemotherapy at AIIMS, New Delhi

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2018/10/016003

Enrollment

Registered

2018-10-12

Start date

Unknown

Completion date

Unknown

Last updated

2021-11-24

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

Conditions

None listed

Interventions

Intervention1: Video based education: Experimental group participants will receive Video based education only once which will be displayed for 13 minutes consisting of ways to prevent infection and m

Eligibility

Inclusion criteria

Inclusion criteria: 1.Caregiver having age >= 18 years 2.Caregiver of a child with acute leukemia undergoing chemotherapy cycle 1 and 2. 3.Caregiver who is able to understand Hindi/English language. 4.Caregivers whose hearing and vision is corrected/not impaired 5.Caregiver who have been living with the child for a period of minimum 1 month and who are available for the study.

Exclusion criteria

Exclusion criteria: 1.Privately hired caregivers 2.Caregivers who do not give consent for the study.

Design outcomes

Primary

Measure	Time frame
There will be a significant difference in the knowledge of caregivers of children with acute leukemia who will receive VBE in addition to routine care as compare to those who will receive only routine care regarding prevention of infection during chemotherapy.Timepoint: 3 Times	—

Secondary

Measure	Time frame
There is an association between the knowledge of caregivers of children with acute leukemia regarding prevention of infection during chemotherapy and selected demographic variables.Timepoint: 3 times, pretest, immediate post test and at 1 month of the intervention	—

Countries

India

Contacts

Public ContactAanchal

All India Institute of Medical Sciences

aaditiprashant@gmail.com8920455490

Outcome results