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A randomized controlled study to evaluate a digital intervention for treating burnout in adults

A randomized controlled study to evaluate a digital intervention for the treatment of burnout in adults

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN75863224
Enrollment
112
Registered
2026-02-02
Start date
2026-02-02
Completion date
Unknown
Last updated
2026-02-16

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

Conditions

Burnout Mental and Behavioural Disorders

Interventions

elona explore is a digital health application that provides patients with mental health disorders (depression, anxiety/panic disorders, OCD, adjustment disorders, burnout, and somatoform disorders) wi

Sponsors

Elona Health GmbH
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: 1. Diagnosed with the following ICD-10 diagnosis: Z73.0: Burnout 2. Over the age of 18 years 3. Sufficient German language skills (in writing and reading) 4. Possess a smartphone (iOS or Android operating system) with internet access 5. Provide signed and dated informed consent 6. Willing to comply with the protocol

Exclusion criteria

Exclusion criteria: All individuals without the included ICD-10 diagnosis, as well as individuals with the following comorbid ICD-10 diagnoses, are excluded: F00-F09: Organic, including symptomatic, mental disorders F10-F19 Mental and behavioural disorders due to psychoactive substance use (except F17.1, F17.2, F17.3) F20-F29: Schizophrenia, schizotypal and delusional disorders F30: Manic episode F31.0, F31.1, F31.2, F31.5, F31.6, F31.8, F31.9: Bipolar disorder current hypomanic or manic episode F32.3: Severe depressive episode with psychotic symptoms F33.3: Recurrent depressive disorder, current episode severe with psychotic symptoms Further exclusion criteria are as follows: 1. Patients who are currently undergoing psychotherapy (at the point of enrollment) 2. Patients who plan to terminate or change the dose of their current medication that was prescribed for a mental health disorder, or those who plan to start taking a prescription medication prescribed for a mental health disorder within the next 10 weeks (a stable dose of medication three months before enrollment in the trial is allowed). 3. Patients who are currently using a digital health application for a mental health disorder (at the point of enrollment) 4. Individuals with acute suicidality (assessed via suicidality screening of the mini-DIPS at the initial screening) 5. If an individual is currently enrolled or is planning to participate in a potentially confounding drug or device trial during the study, enrollment into this study is not possible. 6. If an individual underwent psychotherapy three months prior to enrolling, study participation is not possible. 7. It should be noted that the influence of concomitant treatments (especially psychotherapy) is intended to be reduced. Therefore, patients should not be recruited from an existing waiting list.

Countries

Germany

Contacts

Public ContactAnika Meißner
anika.meissner@uni-goettingen.de+49 (0)5513929022

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 19, 2026