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Evaluation of a PReparatory eHealth intervention for patients in CArdiac REhabilitation: a pilot study.

Evaluation of a PReparatory eHealth intervention for patients in CArdiac REhabilitation: a pilot study. - PReCARE

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON51403
Enrollment
60
Registered
2022-12-07
Start date
2023-02-08
Completion date
Unknown
Last updated
2024-04-09

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

Conditions

Cardiovascular disease Heart disease

Interventions

Patients will be enrolled in the intervention group based on randomization. The intervention group will use an eHealth application during the waiting period before cardiac rehabilitation starts. The

Sponsors

Erasmus MC, Universitair Medisch Centrum Rotterdam
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Patients with a low socio-economic position who are eligible for participation in cardiac rehabilitation and who are referred by their cardiologist to Capri Hartrevalidatie.

Exclusion criteria

Exclusion criteria: Patients with severe physical, psychological, or cognitive impairments.

Design outcomes

Primary

MeasureTime frame
Feasibility of the intervention in terms of usage, acceptability and experience. - Usage will be determined based on the number of days used, length of use (period from first to last day use), number of viewed messages and time spent per visit. - Acceptability will be measured using a self-designed questionnaire (9 items) based on the USE questionnaire (Usability, Usefulness and satisfaction) - Experience will be determined based on a thematic analysis of several qualitative semi-structured interviews.

Secondary

MeasureTime frame
- Patient activation measured using the PAM-13 questionnaire. We use the Dutch translation of this questionnaire consisting of 13 items with a 4-point Likert scale. - Feelings of certainty and guidance using a self-designed questionnaire (9 items).

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)