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The Effect of Education Given to Patients with Atrial Fibrillation on Anxiety Levels

Atriyal Fibrilasyonu Olan Hastalara Verilen Eğitimin Anksiyete Düzeyleri Üzerine Etkisi

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06793319
Enrollment
60
Registered
2025-01-27
Start date
2024-07-01
Completion date
2024-10-31
Last updated
2025-01-27

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

Conditions

Atrial Fibrillation (AF), Atrial Fibrillation New Onset

Keywords

Anxiety, Atrial Fibrillation, Patient education

Brief summary

This study aims to evaluate the effect of a structured training program on state anxiety levels in patients diagnosed with Atrial Fibrillation (AF). AF is a chronic heart rhythm disorder that negatively affects patients' quality of life with both physical and psychological symptoms. Lack of information and uncertainty in AF patients cause increased anxiety levels, making compliance with treatment difficult. This study aims to determine whether an educational intervention for AF patients can reduce their anxiety levels and increase their awareness of the disease. This is a randomized controlled trial. A two-session individual training program containing detailed information about AF will be applied to the training group and no training will be given to the control group. Data will be collected through a personal information form and the Situationality Anxiety Inventory (STAI). Hypotheses of the Research H0: Training regarding Atrial Fibrillation has no effect on the anxiety level of patients. H1: Education regarding Atrial Fibrillation reduces the anxiety level of patients.

Interventions

State Anxiety Inventory was filled out before the training. Atrial Fibrillation training was provided. After the training, the Situationality Anxiety Inventory was filled out again. It was aimed to evaluate the effect of education on anxiety.

Sponsors

Kübra Kocaispir
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
SINGLE (Subject)

Intervention model description

It is a study that does not involve drugs or biological products. It was examined how the education given to patients affected anxiety. The operating model is parallel.

Eligibility

Sex/Gender
ALL
Age
18 Months to 65 Months
Healthy volunteers
No

Inclusion criteria

* Newly diagnosed with AF, * Able to speak and understand Turkish, * Does not have a physical or psychological disorder that would cause communication problems, * Patients between the ages of 18 and 65 who are oriented to place and time, -Agreeing to participate in the study

Exclusion criteria

\* Using any psychotropic medication (antidepressant, anxiolytic, antipsychotic)

Design outcomes

Primary

MeasureTime frameDescription
Anxiety Levels of Patients Given Atrial Fibrillation TrainingWithin 2-3 hours after trainingThis study was conducted in a randomized controlled manner. It was done with 60 patients. 30 patients were assigned to the training group and 30 patients to the control group. There is a training and control group. Groups will fill out a personal information form and the State Anxiety Inventory. Atrial fibrillation training was given to the training group and the state anxiety inventory (STAI 1) was filled out again. The control group was not given any training and had a state anxiety inventory filled out. The data obtained in the study were analyzed using the SPSS (Statistical Package for Social Sciences) for Windows 22.0 program. Number, percentage, mean and standard deviation were used as descriptive statistical methods in the evaluation of the data. Differences between the proportions of categorical variables in independent groups were analyzed with Chi-Square tests. Kurtosis and Skewness values were examined to determine whether the research variables showed normal distribution

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026