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Nursing Intervention for the Acceptance of the Patient to the Cardioverter

Nursing Intervention for the Acceptance of the Patient to the Cardioverter

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12617000451303
Enrollment
72
Registered
2017-03-27
Start date
2017-03-08
Completion date
2017-09-15
Last updated
2018-06-11

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

Conditions

None listed

Brief summary

This research it is proposed to design and apply a nursing intervention, to improve the level of acceptance to device in daily life, Approaching the physical, psychological and social consequences caused by the implantation of the ICD, with the goal that the implanted people achieve the greater benefit of the device, in years of quality survival. The knowledge generated will provide evidence for nursing professionals in relation to the effects of the intervention applied in the pre-implant period and provides new tools for nursing practice in relation to the care of this population group. Hypothesis A Structured Nursing Intervention with two components: educational and relaxation strategies, applied in the pre-implantation period, provides the person the necessary tools to achieve acceptance of the device, reducing the physical, psychological and social consequences of the implantation of the Cardioverter, Allowing the integration of technology into life.

Interventions

The Nursing Intervention APECC “Acceptance In People With Cardiac Stimulation Cardioverter” is a direct attention treatment, based on the knowledge and clinical judgment, that the nurse performs independently in the pre-implantation period, to help the person to Accept the cardiac stimulation device Cardioverter, in response To the physical, psychological and social needs that can appear from the implantation to the performance of the daily functions. The intervention is proposed from the Social

The Nursing Intervention APECC “Acceptance In People With Cardiac Stimulation Cardioverter” is a direct attention treatment, based on the knowledge and clinical judgment, that the nurse performs independently in the pre-implantation period, to help the person to Accept the cardiac stimulation device Cardioverter, in response To the physical, psychological and social needs that can appear from the implantation to the performance of the daily functions. The intervention is proposed from the Social Learning Theory for behavior modeling, these are developed through three components, the first corresponds to an educational component provided by the nurse who is the person that has the knowledge to address the main issues of the implantation and that have been reported in the evidence, such as: 1 What is a cardio-defibrillator, how it acts, how the implantation is performed, what are the indications 2 Physical consequences of implantation to the device: wound care, physical activity, body image change, what can I expect and how can I act? 3 Social Consequences: Changes in the job, family and social role, sexual activity, driving limitations, activities of daily living, What can I expect and how can I act? 4 Psychological Consequences: primary emotions (fear, apprehensiveness, anger, sadness) and Anxiety and Depression. What is normal and how can I act? The second component refers to the modeling of behavior through the peers or people with similar conditions, so those two people who have a cardiodesfibrilador express their experience of living with the device, its advantages and disadvantages and how they settle their difficulties. Through 15 minutes video of two people who have had an implant talking about their experiences is watched in the session. Finally, the last component is an exercise in relaxation that will allow the implanted person to practice it in their moments of anxiety or stress. Are 15 minutes of video with images, music and instructions for the relaxation of body and mind, is watched in the session. The Nursing intervention will be delivered by the nurse face to face, in a single moment with a duration of approximately 60 minutes for the session, be supported using tools such as the educational flipchart designed for this study contains illustrative images to explain the educational content of physical, psychological, social changes and the use of a DVD designed for this study, which contains three small videos of 15 minutes duration, with the components educational, experiences and exercise in relaxation, the study participants can take home, for your consultation anytime you require it. note: The participants will be assigned one by one to each group 30 participants to intervention group 1, persons receiving intervention before to device implantation. 30 participants to intervention group 2, people receiving the intervention once the device is implanted and before clinical discharge. 30 participants to the control group, people receiving standar care.

Sponsors

Diana Marcela Castillo Sierra
Lead SponsorIndividual

Study design

Allocation
Non-randomised trial
Intervention model
Parallel
Primary purpose
Educational / counselling / training
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

-Being over 18 years until 90 years old -Persons with the first time indication of implantation of cardiac stimulation therapy with defibrillation. note: The Participants should not have received the device to be elected for enrolment in this trial.

Exclusion criteria

-People with cognitive disabilities -People with device complications in the post-implant period. -Persons who are not implanted with the Cardioverter device. Clarifying Note: Exclusion criterion number two is established taking into account that people who are implanted with the device can have serious complications that might require additional treatment, a condition that would not allow to continue in the process of the study, since all the Acceptance level measurements should be performed after the implant.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026