RecruitingNANCT07454317

Remote Physical Activity Biofeedback Intervention for Patients With Paroxysmal Atrial Fibrillation Using Mobile Health Technology.

Sponsor: Liverpool John Moores University

Trial Details

ConditionAtrial Fibrillation (Paroxysmal)
InterventionBiofeedback intervention
PhaseNA
StatusRecruiting
Participants40
Est. Completion1 Feb 2028
Last Updated22 May 2026

Primary Outcome

Phase 1: Co-design biofeedback nudges and report content, layout and the optimal time/frequency of nudges. Underpinned by a double diamond framework, through an iterative co-design process.; Phase 1: Co-design biofeedback nudges and report content, layout and the optimal time/frequency of nudges. Underpinned by a double diamond framework, through an iterative co-design process.; Phase 2: Determine the number of patients identified, screened, appraoched eligable, consented, completed the trial, withdrew from the trial, and adherence to the trial.

Eligibility Criteria

Inclusion Criteria

Inclusion Criteria: * Participant is willing and able to give informed consent for participation in the study. * Aged 18 or over. * Diagnosed with paroxysmal AF * Deemed medically stable and well managed. Exclusion Criteria: * Any concurrent cardiac arrhythmia * Blood pressure \>180/100 * Unstable angina * Myocardial infarction within the previous 3 months * Valvular heart disease * Heart failure NYHA class 4 * \<6 months post-transplant * Resting/uncontrolled tachycardia * Stroke in last 6 weeks * Cardiac sarcoidosis * Injury or disability preventing exercise

Trial Sites

Countries

United Kingdom
View Registry Entry

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