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A Self-Management Support Intervention for Patients with Atrial Fibrillation: A Randomized Controlled Pilot-Trial

A Self-Management Support Intervention for Patients with Atrial Fibrillation: A Randomized Controlled Pilot-Trial - PSPAFpilot

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
DRKS
Registry ID
DRKS00012808
Enrollment
20
Registered
2017-09-04
Start date
2017-09-21
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

I48.0 I48.1

Interventions

Group 1: Educational intervention (Pulse self-palpation)
once before hospital discharge Group 2: Usual care

Sponsors

Universitäts-Herzzentrum Freiburg · Bad Krozingen
Lead Sponsor

Eligibility

Sex/Gender
All
Age
35 Years to No maximum

Inclusion criteria

Inclusion criteria: hospitalization; dignosis of paroxysmal or persistent Atrial Fibrillation; residence within a geographical area around Bad Krozingen reachable by car in 25 minutes; able to read, write and understand German

Exclusion criteria

Exclusion criteria: cognitive (e.g. dementia) or physical impairments of both hands (e.g. peripheral polyneuropathy); condition after AV nodal ablation and implanted pacemaker; life expectancy less than two months according to the physician; individuals that already took part in any comparable education program

Design outcomes

Primary

MeasureTime frame
Capability of pulse self-palpation; observation through healthcare provider using a checklist; 2. data collection point (25-35 days after enrollment)

Secondary

MeasureTime frame
Sign and symptom management; dealing with a vignette; 2. data collection point. Adherence: pulse diary; between 1. and 2. data collection point. Feasibility Outcomes: Acceptability of intervention: questionnaire; 1. data collection point. Feasibility of intervention: field notes, audio recordings; during interventions. Feasibility of research methods: checklists, field notes; from date of recruitment to data analysis. Burden of study participation: questionnaire; 2. data collection point. [1. data collection point = day of enrollment/of Intervention] [2. data collection point = 25-35 days after enrollment]

Countries

Germany

Contacts

Public ContactStefan Jobst

Universitäts-Herzzentrum Freiburg · Bad Krozingen

Stefan.Jobst@universitaets-herzzentrum.de+4976334023361

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 27, 2026