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Acceptance of a digital rehabilitation aftercare using CASPAR: a cohort study

Acceptance of a digital rehabilitation aftercare using CASPAR: a cohort study - AcdiReAc

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00030408
Enrollment
200
Registered
2022-10-24
Start date
2022-11-01
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

M00-M99

Interventions

Group 1: Rehabilitants with musculoskeletal diseases from two inpatient rehabilitation clinics in Germany are asked about their acceptance of digital rehabilitation aftercare.

Sponsors

Universität zu Lübeck, Institut für Sozialmedizin und Epidemiologie
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 67 Years

Inclusion criteria

Inclusion criteria: We include patients receiving a rehabilitation due to a musculoskeletal disease. Patients did not start a rehabilitation aftercare already and were able to complete online questionnaires, if necessary, with telephone support.

Exclusion criteria

Exclusion criteria: We exclude patients who used or currently use the CASPAR app during aftercare, and patients who did not provide their email address for a follow-up assessment.

Design outcomes

Primary

MeasureTime frame
Actual use; When? 5-week folllow-up, How? Yes/no, Online questionnaire

Secondary

MeasureTime frame
Intention to use; When? Baseline, 5-week follow-up, How? Continuous, 1 to 7 points, Online questionnaire, German and adjusted version of the TAM3 (Venkatesh & Bala, 2008) Perceived usefulness and perceived ease of use are considered as both dependent and explanatory variables. Perceived usefulness; When? Baseline, 5-week follow-up, How? Continuous, 1 to 7 points, Online questionnaire, adapted from TAM3 (Venkatesh & Bala, 2008) Perceived ease of use; When? Baseline, 5-week follow-up, How? Continuous, 1 to 7 points, Online questionnaire, adapted from TAM3 (Venkatesh & Bala, 2008) Additional explanatory variables were assessed using modified constructs and items of the TAM3 questionnaire (Venkatesh & Bala, 2008). Functional results; When? Baseline, 5-week follow-up, How? Continuous, 1 to 7 points, Online questionnaire, adapted from TAM3 (Venkatesh & Bala, 2008) Support from environment; When? Baseline, How? Continuous, 1 to 7 points, Online questionnaire, adapted from TAM3 (Venkatesh & Bala, 2008) App-related self-efficacy; When? Baseline, 5-week follow-up, How? Continuous, 1 to 7 points, Online questionnaire, adapted from TAM3 (Venkatesh & Bala, 2008) External requirements; When? Baseline, 5-week follow-up, How? Continuous, 1 to 7 points, Online questionnaire, adapted from TAM3 (Venkatesh & Bala, 2008) Enjoyment; When? Baseline, 5-week follow-up, How? Continuous, 1 to 7 points, Online questionnaire, adapted from TAM3 (Venkatesh & Bala, 2008) Computer anxiety; When? Baseline, 5-week follow-up, How? Continuous, 1 to 7 points, Online questionnaire, adapted from TAM3 (Venkatesh & Bala, 2008) Perceived risk; When? Baseline, How? Continuous, 1 to 7 points, Online questionnaire (Wu & Wang, 2004) Perceived flexibility; When? Baseline, 5-week follow-up, How? Continuous, 1 to 7 points, Online questionnaire (own development) Affinity for Technology Interaction; When? Baseline, How? Continuous, 1 to 6 points, Online questionnaire, Affinity for Technology Interaction

Countries

Germany

Contacts

Public ContactJohanna;Matthias Prehn;Bethge

Universität zu Lübeck, Masterstudiengang Gesundheits- und Versorgungswissenschaften;Universität zu Lübeck, Institut für Sozialmedizin und Epidemiologie

johanna.prehn@student.uni-luebeck.de;matthias.bethge@uksh.de+49 45150051280;+49 451 50051280

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026