Skip to content

Daily activities patients post ICD implantation

Effectiveness of an Instructional Program on Patients’ Safe Measures Post Implantable Cardioverter Defibrillator

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20240813062748N1
Enrollment
92
Registered
2024-08-17
Start date
2023-07-23
Completion date
Unknown
Last updated
2024-08-26

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

Conditions

Many patients who receive Implantable Cardioverter Defibrillators (ICDs) lack adequate knowledge and understanding of the necessary safety measures post-implantation. Research indicates that patients often feel that the information provided during their care is insufficient and not tailored to their specific needs. To address this gap.

Interventions

Intervention group: 30 patients (study group) received the pre-test and intervention of instructional program regarding the safe measures and post-test apply after 4 weeks for group..

Sponsors

University of Baghdad\ College of Nursing
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients who had an implantable cardioverter defibrillator device before (3) months and above A patient who has agreed to participate in the study and were able to attend the follow-up regularly Patients with a traditional implantable cardioverter defibrillator device

Exclusion criteria

Exclusion criteria: Hospitalized patients Patients had an amputation Patients who had mental retardation such as (Down syndrome). Patients involved with other studies at the same time as the current study

Design outcomes

Primary

MeasureTime frame
The primary outcome of the study is to evaluate the effectiveness of the instructional program on patients' safety measures regarding the knowledge and practice post-ICD, and optimistic to improve the level of an awareness post the intervention for the study group. Timepoint: pre-test was done for both study and control group and intervention of instructional program implemented for study group and post-test apply after 4 weeks for both groups. Method of measurement: The primary outcome variable was measured using self-report data collection, which was then applied to the statistical analysis of the data.

Countries

Iraq

Contacts

Public ContactMohammed Kadhum Sadiq

College of Nursing \ University of Baghdad

mohammed.sadiq2102p@conursing.uobaghdad.edu.iq+964 770 258 1696

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026