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Patient survey on the usability of the Digital Health Application ViViRA for exercise therapy of nonspecific and degenerative back pain

Patient survey on the usability of the Digital Health Application ViViRA for exercise therapy of nonspecific and degenerative back pain - ViViRA_Survey2024

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00034431
Enrollment
100
Registered
2024-07-31
Start date
2024-08-02
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

ViViRA is a digital health application for the treatment of non-specific and degenerative back pain using digitally mediated movement therapy. Further information on indications is summarized in the DiGA directory of the Federal Institute for Drugs and Medical Devices (BfArM): https://diga.bfarm.de/de/verzeichnis/00387.

Interventions

Group 1: Patients suffering from degenerative and/or non-specific back pain with an indication that qualifies for treatment with the DiGA ViViRA will be asked about the perceived usability of ViViRA.

Sponsors

Vivira Health Lab GmbH
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patients with: • Provided consent to the processing of data to improve the technical functionality, user-friendliness, and further development of the DiGA ViViRA (in accordance with DiGAV, § 4 (2)) • Activation code in use • At least 2 completed exercise sessions in the DiGA ViViRA

Exclusion criteria

Exclusion criteria: Users with test access, no consent according to DiGAV, §4, 2(4)

Design outcomes

Primary

MeasureTime frame
Usability: surveyed using the short form of the mhealth App Usability Questionnaire (MAUQ)

Secondary

MeasureTime frame
Qualitative evaluation of usability: Identification and analysis of barriers and challenges to using ViViRA through additional questions and during interviews.

Countries

Germany

Outcome results

None listed

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