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RecruitingNCT07561255RAEMDUpdated May 1, 2026

Exploratory Investigation of the Acceptance and Utility of 14-day Trial Periods and Application-related Outcome Measurement (AbEM) Within the Routine Prescription of the DiGA Axia.

An interventional study of Test-phase with immediate access and Standard procedure in Spondylitis, Ankylosing and Mobile Phone Use, sponsored by Wuerzburg University Hospital. Recruiting at 7 sites in Germany. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-05-01.

Sponsored by Wuerzburg University Hospital · Not applicable, Interventional, and Supportive care

From the registry’s dates

  • Started Apr 2026; still recruiting 7 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
200
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

This prospective, multicenter, controlled real-world quality management study explores the acceptance and utility of two measures discussed in the context of the German Digital Act (DigiG) for the digital health application (DiGA) Axia: a 14-day trial period and an application-related outcome measurement (AbEM). Patients with axial spondyloarthritis in Axia's indication area who are eligible for prescription in routine care will receive one of two onboarding brochure versions in a 1:1 allocation: either the standard access procedure or immediate 14-day trial access until the health insurance activation code arrives. The manufacturer will analyze aggregated anonymized data to compare voucher redemption and app activation frequencies between groups and to assess acceptance and return rates of a voluntary five-item AbEM questionnaire at weeks 6 and 12. Secondary analyses will descriptively evaluate AbEM results and anonymized usage data.

02

Conditions studied

  • Spondylitis, Ankylosing
  • Mobile Phone Use

Keywords

  • axial spondyloarthritis
  • mobile health
  • digitalization
  • onboarding
  • real-world
  • therapeutic app
03

In context

Spondylitis, Ankylosing

531 studies on the registry are indexed under Spondylitis, Ankylosing; 98 are open to participants now.

This study's planned enrollment of 200 is above the median of 88 across 302 interventional studies indexed under Spondylitis, Ankylosing.

Browse Spondylitis, Ankylosing studies →

Lead sponsor

Wuerzburg University Hospital is the lead sponsor of 98 studies on the registry; 19 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Willingness to use Axia.
  • Axia indication area.
  • Willingness to activate via onboarding brochure.

Exclusion criteria

Exclusion Criteria:

  • Absence of the inclusion criteria
05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Care provider)
Enrollment
200 participants (estimated)

Study arms

  • Experimental
    Immediate app-use by a test phase

    Device: Test-phase with immediate access

  • Active comparator
    Standard procedure

    Other: Standard procedure

Interventions

  • DeviceTest-phase with immediate access

    Use of two versions of an onboarding brochure in A7 format containing a QR code. The brochures are provided free of charge to the study centers by the manufacturer. Each study center receives 20 cards in a 1:1 ratio. One version contains the QR code with instructions and support for the standard procedure (Axia can only be used once the activation code has been provided by the health insurance fund). The second version contains a QR code through which Axia can be downloaded from the app store and used with a 14-day trial access until the activation code from the health insurance fund arrives.

  • OtherStandard procedure

    Axia can only be used once the activation code has been provided by the health insurance fund

06

What researchers measure

Primary outcomes

  1. Percentage of participants with successful Axia app activation within 12 weeks, assessed by successful redemption of the activation code

    Successful app activation is defined as successful redemption of the activation code by the participant. The outcome measure is the percentage of participants with successful app activation from baseline through week 12.

    Time frame: 12 weeks

Secondary outcomes

  1. Percentage of participants with a voluntarily completed application-related success measurement questionnaire (AbEM)

    Voluntary completion of the AbEM questionnaire is defined as submission of a completed application-related success measurement questionnaire by the participant.

    Time frame: 6 and 12 weeks

  2. Mean AbEM questionnaire item scores among participants with a completed AbEM questionnaire

    The AbEM questionnaire consists of 6 items assessing application-related success. One item assesses improvement in health status using a 7-point Likert scale. Five items assess the quality of the DiGA using numerical rating scales ranging from 0 to 10, with higher scores indicating better perceived quality. Item scores will be summarized descriptively among participants with a completed AbEM questionnaire.

    Time frame: 6 and 12 weeks

  3. Exploratory analysis of anonymized usage data.

    App usage days are defined as calendar days on which at least one app usage event is recorded for a participant. The total number of app usage days per participant from baseline through week 12 will be assessed using app usage log data and summarized descriptively.

    Time frame: 12 weeks

07

Study locations

7 of 7 sites recruiting
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 1, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07561255
Lead sponsor
Wuerzburg University Hospital
Responsible party
Patrick-Pascal Strunz (PD. Dr. med., Wuerzburg University Hospital) — Principal investigator
First posted
May 1, 2026
Start date
Apr 10, 2026
Primary completion
Dec 31, 2026 (estimated)
Completion
Apr 10, 2027 (estimated)
Last update
May 1, 2026

Study contacts

Patrick-Pascal Strunz, MD
Contact
Strunz_p@ukw.de
093120140100
Patrick-Pascal Strunz
Contact
Strunz_p@ukw.de
093120140100

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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