Skip to content

NURSE-led Follow-up in Patients Undergoing CATheter Ablation for Atrial Fibrillation

Assessing the Nurse-led Educational Intervention in Patients Undergoing Catheter Ablation for Atrial Fibrillation: a Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05333445
Acronym
NURSECAT-AF
Enrollment
66
Registered
2022-04-19
Start date
2022-04-15
Completion date
2024-04-30
Last updated
2025-03-07

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

Conditions

Atrial Fibrillation

Keywords

atrial fibrillation, nurse-led, educational intervention, risk factors, quality of life

Brief summary

The study aims to examine the effect of nurse-led education program on quality of life, atrial fibrillation (AF) risk factors, AF symptomatology, arrhythmia recurrence rate, and readmission rate after AF catheter ablation.

Interventions

BEHAVIORALeducational program

Education for the management of AF is carried out in a structured way, following the Bowyer model using the following pre-specified subtitles: How the heart works; Causes and risk factors of AF; Symptoms of AF; Goals of treatment in atrial fibrillation ; ''preparation for the ablation procedure''; and Lifestyle Modification. The technique consists of discussing the main subtitles and adapting the visit line to the needs of each patient

BEHAVIORALrisk factors management

identify risk factors and offer guidance based on management strategies for the specific risk factor in each case

BEHAVIORALtelephone and e-mail contact

patients will also be provided with a phone number and email to contact the nurse for any concerns outside the designated times within the twelve-month follow-up.

OTHERusual care

standard care

Sponsors

Hospital Clinic of Barcelona
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Derivatives from the outpatient clinic of the center itself, as well as patients referred from other centers that have ours as a reference for a first AF ablation procedure. * Have signed the informed consent.

Exclusion criteria

* Patients with cognitive impairment or disorientation. * Patients with problems of comprehension or expression of Spanish or Catalan. * Patients who are part of the medical or nursing group. * Patient with defined heart failure with a left ventricular ejection fraction (LVEF) less than 40% and a NYHA III or IV.

Design outcomes

Primary

MeasureTime frameDescription
changes from the baseline and better score in the validated ASTA questionnaire of the intervention group compared to the control group at 12 months in quality of life of patients .12 monthsWe will use the second part of ASTA questionnaire: it consists of 13 questions and the answers are measured using a Likert frequency scale from Never = 0 to Always = 4. Higher scores on this scale represent poorer quality of life.

Secondary

MeasureTime frameDescription
number of participants with re-hospitalisation or emergency room visits for cardiovascular cause12 monthsdifferences between the two groups in number of patients who come to the emergency room or re-admit after discharge from catheter ablation.
number of participants with recurrences at AF rhythm12 monthsnumber of AF detected by ECG or 24-hour cardiac holter routine at 3, 6 and 12 months.
differences between both groups in the score received by the patients in the User Experience Questionnaire based on the Picker-33 Patient Experience Questionnaire3 monthsIt consists of 14 closed-ended questions and is performed using a checklist to assign numerical values to subjective satisfaction using a Likert scale from No = 0 to Yes, always = 4. Higher scores on this scale represent greater satisfaction. An open question has been added so that participants can add their suggestions
number of patients who have the AF risk factor within normal parameters12 monthsdifferences between the two groups in number of patients with BMI and/or waist circumference changes from the baseline, better score on the Minnesota Adapted Scale for Physical Exercise, number of patients who do not smoke or drink alcohol, number of patients with positive polysomnography, number of patients with impaired of the analytical parameters of HbA1c, TSH, LDL or Triglycerides.
differences between both groups in the score obtained in the adapted AFKAT questionnaire patient's knowledge of AF.3 monthsdifferences between both groups in the Level of knowledge of FA through the AFKAT questionnaire validated in English but adapted and translated into Spanish by our team. It consists of 25 questions with dichotomous True/False answers. The more true answers, the better knowledge the participant has.
calls and emails received12 monthsQuantify the calls and emails received from patients to the FA nurse.
Differences between both groups in intensity, frequency and severity of symptoms related to AF evaluated with the validated ASTA questionnaire12 monthsdifferences between both groups in the score obtained in the first part of the validated questionnaire in Spanish and English sensitive for patients with AF. It will be self-filled by the patient himself. It consists of 8 questions formulated in 3 different ways: (1) Multiple correct answer multiple choice questions. (2) Multiple choice questions with only one correct answer. (3) Checklist for assigning numerical values to frequency using a Likert scale from Never = 0 to Always = 4. Higher scores on this scale represent greater severity of symptoms.

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 27, 2026