Effectiveness of a structured educational intervention on registered nurses’ knowledge, attitudes, and practices toward adherence to pressure injury prevention

ISRCTN ISRCTN14515418
DOI https://doi.org/10.1186/ISRCTN14515418
Sponsor King Saud University
Funder King Saud University
Submission date
19/12/2025
Registration date
05/01/2026
Last edited
05/01/2026
Recruitment status
No longer recruiting
Overall study status
Completed
Condition category
Other
Prospectively registered
Protocol
Statistical analysis plan
Results
Individual participant data
Record updated in last year

Plain English summary of protocol

Not provided at time of registration

Contact information

Mr Mousa Asiri
Principal investigator, Public, Scientific

Saudi Arabia
Riyadh
11411
Saudi Arabia

ORCiD logoORCID ID 0000-0003-2119-1400
Phone +966 546668220
Email Maseri@psmmc.med.sa

Study information

Primary study designInterventional
AllocationRandomized controlled trial
MaskingBlinded (masking used)
ControlPlacebo
AssignmentParallel
PurposePrevention
Scientific titleEffectiveness of a structured educational intervention on registered nurses’ knowledge, attitudes, and practices toward adherence to pressure injury prevention: a two-arm randomized controlled trial
Study objectivesTo assess the efficacy of a structured, evidence-based educational intervention on registered nurses' performance in pressure injury prevention relative to regular education.
Ethics approval(s)

Approved 01/07/2025, Institutional Review Board of Prince Sultan Military Medical City (Saudi Arabia, Riyadh, 11411, Saudi Arabia; +966 546668220; ethical@psmmc.med.sa), ref: E-2601

Health condition(s) or problem(s) studiedRegistered nurses’ knowledge, attitudes, and practices toward adherence to pressure injury prevention
InterventionThis study used a parallel-group, two-arm randomized controlled trial (RCT) to assess the efficacy of a structured educational intervention on registered nurses' knowledge, attitudes, and practices (KAP) regarding adherence to pressure injury prevention (Asiri et al., 2025). Nurses who met the eligibility criteria were randomly assigned in a 1:1 ratio to either an intervention group, which received a comprehensive, evidence-based program for pressure injury prevention education, or a control group, which received routine instruction (Houser & Oja, 2025; Potter et al., 2025). Randomization was performed using a computer-generated random sequence, with allocation concealment ensured by sequentially numbered, opaque, sealed envelopes (Clark et al., 2021). Participant blinding was impractical given the characteristics of the educational intervention; however, outcome evaluation and data analysis were conducted using standardized protocols to reduce bias (Melnyk & Morrison-Beedy, 2018). The outcomes were assessed at baseline for the intervention group and weekly for the routine group using validated instruments that evaluated knowledge, attitudes, and practices related to adherence to pressure injury prevention (Melnyk & Morrison-Beedy, 2018). The trial was executed in compliance with Good Clinical Practice standards and is documented in accordance with the CONSORT guidelines for randomized controlled trials (Hopewell et al., 2025).
Intervention typeOther
Primary outcome measure(s)
  1. Nurses’ adherence to pressure injury prevention measured using a validated adherence questionnaire (QARPPU) at baseline and immediately post-intervention
Key secondary outcome measure(s)
  1. Nurses’ knowledge of pressure injury prevention measured using the Pressure Ulcer Knowledge Assessment Tool (PUKAT-2) at baseline and immediately post-intervention
  2. Nurses’ self-reported pressure injury prevention practices measured using the Practice questionnaire (Thomas & Nain, 2023) at baseline and immediately post-intervention
Completion date01/12/2025

Eligibility

Participant type(s)
Age groupAdult
Lower age limit22 Years
Upper age limit60 Years
SexAll
Target sample size at registration250
Total final enrolment222
Key inclusion criteria1. Registered nurses who delivered direct patient care in the participating units
2. Minimum of one year of clinical experience in the nursing department of the same facility
3. Nurses are prepared to grant informed consent
Key exclusion criteria1. On prolonged leave during the research duration
2. Intended to relocate from the unit during subsequent evaluation
3. Had undergone similar organized pressure injury prevention training during the last six months
4. Did not provide direct care to patients
Date of first enrolment15/07/2025
Date of final enrolment15/07/2025

Locations

Countries of recruitment

  • Saudi Arabia

Study participating centre

Prince Sultan Military Medical City
Saudi Arabia
Riaydh
11411
Saudi Arabia

Results and Publications

Individual participant data (IPD) Intention to shareNo
IPD sharing plan summaryNot expected to be made available
IPD sharing plan

Editorial Notes

05/01/2026: Study's existence confirmed by the Institutional Review Board of Prince Sultan Military Medical City.