Effectiveness of Interventional package on prevention of pressure ulcers.
- Conditions
- Diseases of the nervous system,
- Registration Number
- CTRI/2021/07/034794
- Lead Sponsor
- A Dipomala Devi
- Brief Summary
Participants will be enrolled once ethical clearance is obtained. informed consent will be taken and baseline data will be collected followed by video-assisted teaching intervention will provide to the experimental group whereas the control group will be receiving routine care.
post-test knowledge will be tested immediately after the intervention and after the 8th week of intervention.
the experimental group will be receiving a log sheet to maintain in the home which will be assessed once in every week.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not Yet Recruiting
- Sex
- All
- Target Recruitment
- 115
Caregivers of adult patients with severe neurological disability with a mRS score of more than or equal to 4 irrespective of the aetiology, Patients above 18yrs of age, Willing to participate in the study.
Patients aged less than 18 years Caregivers who don’t know Hindi or English Patients with other uncontrolled co-morbidities Patient’s condition improves to mRS of less than or equal to 3 in period of follow up then the participants will be removed.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The primary outcomes of the trial will be a reduction in incidence of pressure ulcer from 30% to 18% (12% absolute result) with 90% CI and level of significance at 0.05. 6 MONTHS
- Secondary Outcome Measures
Name Time Method Severity of pressure ulcers will not proceed from grade 2 to grade ≥ 3 Knowledge
Trial Locations
- Locations (1)
AIIMS, NEW DELHI
🇮🇳South, DELHI, India
AIIMS, NEW DELHI🇮🇳South, DELHI, IndiaA Dipomala DeviPrincipal investigator7678314311missdipomala@gmail.com