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NCT Number: NCT06575582

Digital Navigators for Acceptance and Competence Development with Mental Health Apps

The goal of this clinical trial is to learn if and how so called "Digital Navigators" (DN) can help general practitioners, outpatient psychiatrists and psychologists as well as their treated patients to use digital mental health apps (DiGAs) and integrate it into their treatment. The main questions it aims to answer are:

* What are the chances and implementation barriers of DN? * What are the acceptance and expectations towards DN? * Do DN affect the psychological health of patients? * Do DN affect the digital health literacy and technical competence of participants?

Employees of medical teams (e.g. medical assistants) receive training to become a DN. Afterwards patients are accompanied and supported by the DN for 12 weeks to select and use a suitable app for their mental disorder.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Praxis Brandenburg an der Havel, Brandenburg an der Havel, Brandenburg, Germany

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About this study

The study aims to promote the use of digital health applications (DiGAs) to improve mental health and provide timely treatment for underserved populations. Currently, DiGAs are only used by a small proportion of patients and practitioners in Germany. In order to solve this care problem, employees of medical teams, such as medical assistants, are to be trained as so-called 'digital navigators'. These digital navigators support stakeholders in the selection and use of mental health apps, impart the necessary digital skills, improve adherence and relieve the burden on those providing treatment.

As part of the pilot project, digital navigators will be implemented as an example in GP and outpatient psychiatric care in a rural region of Brandenburg. Firstly, a preliminary study will be conducted to determine the acceptance and expectations of the digital navigators using interviews and focus groups. The researchers then complete a training program at Harvard Medical School and adapt the 'Harvard Digital Navigator Training' to the German framework conditions. This adaptation process is supported by discussion groups with patients and practitioners.

In the next step, medical assistants in six study centres will receive the adapted training. A central tool available to them is the DiGAnavigator.de website, a guide for DiGAs. The digital navigators help with the integration of DiGAs into the treatment of 48 patients with mental illnesses and accompany them over a period of 12 weeks.

Finally, the implementation will be evaluated. The evaluation analyses the implementation hurdles and the effects on the eHealth literacy of patients and professionals. The eHealth Literacy Scale (eHeals) and the Digital Health Literacy Index (DHLI) will be used for this purpose. An accompanying process evaluation analyses the acceptance, effects and implementation barriers of the digital navigators. In addition, both patients and staff are surveyed regarding their digital and technical skills as well as their willingness and ability to change before and after the intervention. Furthermore, the severity of the patients' illness will be recorded and compared before and after the intervention using validated scales. To ensure sustainable implementation, the long-term aim is to provide accredited training to become a digital navigator.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Main diagnosis according to ICD 10 F00-F69, F80-F99
  • Capacity to consent is given
  • Sufficient language skills for an interview in German
  • Participants have access to modern digital hardware (smartphone)
  • Basic knowledge of how to operate a smartphone

Exclusion criteria

  • Acute danger to self or others
  • Patients have received prompt (<= 3 weeks) qualified psychiatric or psychotherapeutic treatment
  • Severe organic brain diseases with cognitive deficits
  • Intellectual disability

Treatment and study plan

Support from Digital Navigators to Treatment Team

Behavioral

The trained professionals (the Digital Navigators) support the treatment teams in the study centers in the selection and integration of suitable apps and digital health applications (DiGAs).

Support from Digital Navigators to Patients

Behavioral

The trained professionals (the Digital Navigators) accompany and support the selected patients to find a suitable app for them and integrate it into their treatment.

Training for Digital Navigators

Behavioral

The training takes place in the six study centers and is preferably aimed at medical assistants.

Primary outcomes

  1. Digital health literacy (focus: digital information retrieval skills)

    Time frame: Before (T0) and after completion of the 12-week intervention (T1)

    Using the self-report rating inventory eHealth Literacy Scale (eHeals). Total score ranges from 8 to 40, with higher scores representing higher self-perceived eHealth literacy.

  2. Digital health literacy (focus: digital interactive skills)

    Time frame: Before (T0) and after completion of the 12-week intervention (T1)

    Using a performance-based rating inventory Digital Health Literacy Index (DHLI). Total score ranges from 0 to 7, with higher scores representing a greater ability to operate digital devices and read and write in web-based modes.

  3. Acceptance towards Digital Navigators

    Time frame: Before the intervention (T0)

    Qualitative questions using semi-structured interviews

  4. Expectations towards Digital Navigators

    Time frame: Before the intervention (T0)

    Qualitative questions using focus groups

  5. Expectations towards Digital Navigators

    Time frame: Before the intervention (T0)

    Qualitative questions using semi-structured interviews

  6. Acceptance towards Digital Navigators

    Time frame: Before the intervention (T0)

    Qualitative questions using focus groups

Secondary outcomes

  1. Willingness and competence to change

    Time frame: Before (T0) and after completion of the 12-week intervention (T1)

    Using the self-report rating inventory "Readiness for Change". Total score ranges from 0 to 172, with higher scores representing higher self-perceived willingness and competence to change.

  2. Digital competence

    Time frame: Before (T0) and after completion of the 12-week intervention (T1)

    Using the self-report rating inventory ICT Self-Concept Scale. Total score ranges from 25 to 150, with higher scores representing higher self-perceived digital competence.

  3. Technical competence

    Time frame: Before (T0) and after completion of the 12-week intervention (T1)

    Using the self-report rating inventory "Kurzskala Technikbereitschaft" (TB, technology commitment). Total score ranges from 12 to 60, with higher scores representing higher self-perceived technical competence.

  4. Psychological Health of Patients (level of functioning)

    Time frame: After completion of the 12-week intervention (T1)

    Using the self-report rating inventory Global Assessment of Functioning (GAF). Total score ranging from 0-100, with a higher score indicating a higher level of functioning.

  5. Psychological Health of Patients (symptom severity, treatment response and the efficacy of treatment)

    Time frame: Before (T0) and after completion of the 12-week intervention (T1)

    Using the self-report rating inventory Clinical Global Impression (CGI); Measuring three dimensions: severity of illness (score 1-7, with a higher score indicating a more severe illness), global improvement (score 1-7, with a higher score indicating a worsening of symptoms) and efficacy (measured with 4×4 rating scale (ranging from 01 - 16) that assesses the therapeutic effect of treatment and associated side effects; e.g. 01 = no side effects; vast improvement; 16 = severe side effects; unchanged or worse condition)

  6. Psychological Health of Patients (depressive symptoms; self-report)

    Time frame: Before (T0) and after completion of the 12-week intervention (T1)

    Using the self-report rating inventory Beck's Depression Inventory (BDI); Total score 0-63, with higher scores representing more severe depressive symptoms.

  7. Psychological Health of Patients (depressive symptoms; clinician-administered)

    Time frame: Before (T0) and after completion of the 12-week intervention (T1)

    Using the clinician-administered rating inventory Hamilton Depression Scale (HAMD); Total score 0-52, with higher scores representing more severe depressive symptoms.

  8. Psychological Health of Patients (anxiety)

    Time frame: Before (T0) and after completion of the 12-week intervention (T1)

    Using the clinician-administered rating inventory Hamilton Anxiety Scale (HAMA); Total score 0-56, with higher scores representing more severe anxiety symptoms.

  9. Psychological Health of Patients (insomnia)

    Time frame: Before (T0) and after completion of the 12-week intervention (T1)

    Using the self-report rating inventory Insomnia Severity Index (ISI); Total score 0-28, with higher scores representing more severe insomia symptoms.

  10. Identification of implementation barriers to the introduction of digital navigators

    Time frame: After completion of the 12-week intervention (T1)

    Qualitative questions using semi-structured interviews

  11. Identification of implementation barriers to the introduction of digital navigators

    Time frame: After completion of the 12-week intervention (T1)

    Qualitative questions using focus groups

  12. Use of Digital Health Applications and the effects of counseling and support by Digital Navigators

    Time frame: After completion of the 12-week intervention (T1)

    Qualitative questions using semi-structured interviews

  13. Use of Digital Health Applications and the effects of counseling and support by Digital Navigators

    Time frame: After completion of the 12-week intervention (T1)

    Qualitative questions using focus groups

Study contacts

Contact information is provided by the study sponsor or research team.

Julian Schwarz, MD

CONTACT

[email protected]

+49 (0) 33638 83501

Sponsors and collaborators

Lead sponsor

Medizinische Hochschule Brandenburg Theodor Fontane

Other

Collaborators

  • Hannover Medical School
  • Harvard Medical School (HMS and HSDM)

Registry information

Acronym: DigiNavi

Important dates

Study start
2024
Primary completion
2025
Study completion
2025
First posted
Aug 28, 2024
Registry last updated
Sep 3, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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