National deployment of RUPERT, an online forum for mental health in the German rescue service

Organizational Data

DRKS-ID:
DRKS00031648
Recruitment Status:
Recruiting complete, study complete
Date of registration in DRKS:
2023-04-28
Last update in DRKS:
2024-03-13
Registration type:
Prospective

Acronym/abbreviation of the study

RUPERT

URL of the study

http://www.rupert-community.de/studie

Brief summary in lay language

Depression is a serious mental disorder that causes substantial suffering. In Germany, approximately one in five adults will suffer from depression at some point in their lifetime. In addition to genetic factors, risk factors for the occurrence of depression include a high level of stress and the frequent experience of extremely stressful events. Emergency medical personnel (EMP) are particularly exposed to these risk factors due to their job. It can therefore be assumed that they have an increased risk of developing depression. More than half of the employees in medical rescue sector are male. Studies indicate that men in particular show unfavourable help-seeking behaviour for mental health-related problems. One explanation for this is the social role perception of men as “strong” and “resilient”. Consequently, mental suffering in men is considered as socially unacceptable and is accordingly associated with stigma. This stigmatisation can have an even higher impact if it meets a traditionally male-dominated organisational culture with rigid masculinity norms, as it can still prevail in the emergency services. As a result, the help-seeking behaviour of both genders can be inhibited to such an extent that available health care offers are not taken up at all or not at an early stage. However, early treatment of depression is important to increase the chance of an uncomplicated, mild course of the disease and to minimize the risk of relapse. This requires suitable and low-threshold care services that are tailored to the needs of the target group. This is the point of departure for the RUPERT project. The aim of the current study is conducting a national roll-out of the RUPERT intervention in Germany. We will analyze whether an implementation strategy that includes regional alliances against depression is superior to the implementation via national communication channels only. We will also investigate the social networks within the digital community of RUPERT, make contact with stakeholders in the rescue services to understand the added value of RUPERT, and explore ideas about generalizing RUPERT to other first responders by interviewing police officers and firefighters.

Brief summary in scientific language

Emergency medical personnel (EMP) are at risk for depressive disorders, as they experience several risk factors such as high job-related strain and frequent exposure to traumatic situations during their work. In addition, some EMP may be little receptive for secondary preventive measures and professional treatment. In particular, males have been shown to struggle with help-seeking for mental health related problems due to their social role perception, norms of masculinity, and fear of stigmatization. Through assuring anonymity, digital interventions can facilitate informal and professional help-seeking for depression. In this context, online self-help forums are a promising approach, as they offer easily accessible information and community-based first help. The RUPERT project aims to create, implement, and evaluate an online intervention for depression, offering psychoeducational information and community-based support through a discussion forum to EMP. The objective of the current study is to conduct a national roll-out of the RUPERT intervention in Germany. Utilizing an effectiveness-implementation hybrid type 2 design, we will i) explore the social networks within the discussion forum and the content shared among the participants using mixed-method content analysis and social network analysis, and we will ii) compare different implementation strategies (regionally targeted vs. nationwide) regarding adoption and penetration of the intervention. Secondary aims are to explore whether the RUPERT intervention can be generalized to other groups of first responders and to collect feedback from multipliers and stakeholders regarding their engagement with RUPERT and the added value for the employers in the rescue service.

Health condition or problem studied

ICD10:
F32 - Depressive episode
ICD10:
F43.2 - Adjustment disorders
ICD10:
Z73 - Problems related to life-management difficulty
Healthy volunteers:
Yes

Interventions, Observational Groups

Arm 1:
The strategy for implementing RUPERT consists of nationwide elements (e.g. press releases, social media activities), in addition there will be targeted regional activities that are carried out by the local alliances against depression in cooperation with local stakeholders in the rescue service. All participants get access to the RUPERT intervention, a digital information and exchange program that includes an information platform and a discussion forum. Data collection takes six months. During this time, log data of the RUPERT intervention will be collected (number of new registrations per region, number and content of posts in the discussion forum, number and duration of page views) and participants will be asked once a month via self-report questionnaire regarding their use of the discussion forum (qualitative, structured questionnaire) and their mental health (PHQ-4, WHO-5).
Arm 2:
The strategy for implementing RUPERT consists of nationwide elements (e.g. press releases, social media activities). All participants get access to the RUPERT intervention, a digital information and exchange program that includes an information platform and a discussion forum. Data collection takes six months. During this time, log data of the RUPERT intervention will be collected (number of new registrations per region, number and content of posts in the discussion forum, number and duration of page views) and participants will be asked once a month via self-report questionnaire regarding their use of the discussion forum (qualitative, structured questionnaire) and their mental health (PHQ-4, WHO-5).

Endpoints

Primary outcome:
Primary implementation outcome: adoption and penetration of RUPERT in different regions (measure: number of new registrations for RUPERT in each region; assessment method: self-report data, registry data on the number of emergency medical personnel in different regions of Germany). Primary clinical outcomes: number of bidirectional interactions established among participants of RUPERT, quantity and quality of the content shared in terms of information and support (assessment method: structured qualitative survey).
Secondary outcome:
Secondary outcome measures are log data of the usage of RUPERT (number of accesses, duration of usage, number of users), sociodemographic characteristics of users, symptoms of depression and anxiety (PHQ-4), and wellbeing of participants (WHO-5). Further outcomes include the feasibility and acceptability of RUPERT (assessed via a structured questionnaire with stakeholders), and the potential of generalising RUPERT to other groups of first responders (assessed via qualitative interviews with police officers and firefighters).

Study Design

Purpose:
Prevention
Allocation:
Non-randomized controlled study
Control:
  • Active control (effective treatment of control group)
Phase:
N/A
Study type:
Interventional
Mechanism of allocation concealment:
No Entry
Blinding:
No
Assignment:
Other
Sequence generation:
No Entry
Who is blinded:
No Entry

Recruitment

Recruitment Status:
Recruiting complete, study complete
Reason if recruiting stopped or withdrawn:
No Entry

Recruitment Locations

Recruitment countries:
  • Germany
Number of study centers:
Monocenter study
Recruitment location(s):
  • Other Landkreis Rosenheim Chiemsee
  • Other Stadt Erlangen, Landkreis Erlangen-Höchstadt Erlangen
  • Other Stadt Essen Essen
  • Other Landkreis Fulda Fulda
  • Other Landkreis Gotha Gotha
  • Other Landkreis Hildesheim Hildesheim
  • Other Landkreis Görlitz Görlitz
  • Other Stadt Leipzig, Landkreis Leipzig Leipzig
  • Other Landkreis Olpe, Landkreis Siegen-Wittgenstein Siegen
  • Other Landkreis Rotenburg (Wümme) Rotenburg (Wümme)
  • Other Landkreis Offenbach Seligenstadt
  • Other Landkreis Northeim, Landkreis Göttingen Göttingen
  • Other Region Weser-Ems Oldenburg
  • Other Landkreis Schaumburg Bückeberg

Recruitment period and number of participants

Planned study start date:
2023-05-01
Actual study start date:
2023-05-04
Planned study completion date:
2024-03-01
Actual Study Completion Date:
2024-03-01
Target Sample Size:
500
Final Sample Size:
83

Inclusion Criteria

Sex:
All
Minimum Age:
18 Years
Maximum Age:
no maximum age
Additional Inclusion Criteria:
Currently employed or voluntarily working as emergency medical personnel or emergency medical technicians; OR rescue service stakeholders and multipliers such as alliances against depression, or any organization of rescue work and service; OR police officers and police personnel working in the field (i.e., exposed to the external environment); fire-fighters, and fire-fighting personnel working in the field (i.e, exposed to the external environment).

Exclusion Criteria

Private individuals or organisations that do not belog to the group of professional first responders.

Addresses

Primary Sponsor

Address:
Stiftung Deutsche Depressionshilfe und Suizidprävention
Prof. Dr. Ulrich Hegerl
Goerdelerring 9
04109 Leipzig
Germany
Telephone:
+49 341 223874-41
Fax:
No Entry
Contact per E-Mail:
Contact per E-Mail
URL:
https://www.deutsche-depressionshilfe.de
Investigator Sponsored/Initiated Trial (IST/IIT):
Yes

Contact for Scientific Queries

Address:
Forschungszentrum Depression der Stiftung Deutsche Depressionshilfe c/o Universitätsklinikum Frankfurt am Main
Dr. Hanna Reich de Paredes
Klinik für Psychiatrie, Psychosomatik und Psychotherapie/ Heinrich-Hoffmann-Str. 10
60528 Frankfurt am Main
Germany
Telephone:
+49 69 6301863-41
Fax:
No Entry
Contact per E-Mail:
Contact per E-Mail
URL:
https://www.deutsche-depressionshilfe.de/forschungszentrum

Contact for Public Queries

Address:
Forschungszentrum Depression der Stiftung Deutsche Depressionshilfe c/o Universitätsklinikum Frankfurt am Main
Dr. Hanna Reich de Paredes
Klinik für Psychiatrie, Psychosomatik und Psychotherapie/ Heinrich-Hoffmann-Str. 10
60528 Frankfurt am Main
Germany
Telephone:
+49 69 6301863-41
Fax:
No Entry
Contact per E-Mail:
Contact per E-Mail
URL:
https://www.deutsche-depressionshilfe.de/forschungszentrum

Principal Investigator

Address:
Forschungszentrum Depression der Stiftung Deutsche Depressionshilfe c/o Universitätsklinikum Frankfurt am Main
Dr. Hanna Reich de Paredes
Klinik für Psychiatrie, Psychosomatik und Psychotherapie/ Heinrich-Hoffmann-Str. 10
60528 Frankfurt am Main
Germany
Telephone:
+49 69 6301863-41
Fax:
No Entry
Contact per E-Mail:
Contact per E-Mail
URL:
https://www.deutsche-depressionshilfe.de/forschungszentrum

Sources of Monetary or Material Support

Private sponsorship (foundations, study societies, etc.)

Address:
Movember Foundation e. V. c/o Preu Bohlig & Partner Rechtsanwälte mbB
Leopoldstr. 11a
80802 München
Germany
Telephone:
No Entry
Fax:
No Entry
Contact per E-Mail:
Contact per E-Mail
URL:
No Entry

Ethics Committee

Address Ethics Committee

Address:
Ethikkommission des Fachbereichs Medizin Universitätsklinikum der Goethe-Universität c/o Universitätsklinikum
Theodor-Stern-Kai 7, Haus 1, 2. OG, Zimmer 207-211
60590 Frankfurt/Main
Germany
Telephone:
+49-69-63017239
Fax:
No Entry
Contact per E-Mail:
Contact per E-Mail
URL:
http://www.kgu.de/ueber-uns/vorstand-des-universitaetsklinikums/dekan/ethikkommission

Vote of leading Ethics Committee

Vote of leading Ethics Committee
Date of ethics committee application:
2023-02-24
Ethics committee number:
2023-1193
Vote of the Ethics Committee:
Approved
Date of the vote:
2023-04-26

Further identification numbers

Other primary registry ID:
No Entry
EudraCT Number:
No Entry
UTN (Universal Trial Number):
No Entry
EUDAMED Number:
No Entry

IPD - Individual Participant Data

Do you plan to make participant-related data (IPD) available to other researchers in an anonymized form?:
Yes
IPD Sharing Plan:
Individual participant data that underlie the results reported in the article(s) will be shared after deidentification. The analytic code will also be made available. The data can be downloaded from https://www.psycharchives.org/ for an unlimited period of time after publication of the article.

Study protocol and other study documents

Study protocols:
No Entry
Study abstract:
No Entry
Other study documents:
No Entry
Background literature:
No Entry
Related DRKS studies:
DRKS00029917 - Analysis of the Mechanisms of Change of the RUPERT intervention

Publication of study results

Planned publication:
No Entry
Publikationen/Studienergebnisse:
No Entry
Date of first publication of study results:
No Entry
DRKS entry published for the first time with results:
No Entry

Basic reporting

Basic Reporting / Results tables:
No Entry
Brief summary of results:
No Entry