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Effectiveness and Equivalence of an Internet-based Virtual Classroom Intervention for Psychosomatic Aftercare

Primary Purpose

Psychosomatic Disorder, Mental Disorder

Status
Completed
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
Curriculum Hannover
Sponsored by
Dr. Becker Hospital Group
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Psychosomatic Disorder focused on measuring Rehabilitation, Psychosomatics, Aftercare, webbased aftercare therapy

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Patients after psychosomatic rehabilitation
  • indication for outpatient psychosomatic aftercare are included in both studies.
  • access to a standard PC and broadband internet connection is required (DSL or LTE).

Exclusion Criteria:

Persons who are

  • are discharged with a capacity of less than three hours per day on the general labour market,
  • receive or have applied for a pension of at least two-thirds of the full pension,
  • receive a benefit that is regularly paid until the start of an old-age pension.
  • suffering from acute addiction disorder / acute psychosis

Sites / Locations

  • Dr. Becker Hospital Group

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Active Comparator

No Intervention

Active Comparator

Active Comparator

Arm Label

Intervention group 1

Control group

Intervention group 2

face-to-face aftercare

Arm Description

webbased aftercare

care as usual

webbased aftercare

face-to-face aftercare

Outcomes

Primary Outcome Measures

change of psychic and somatoform complaints
according to the HEALTH-49 (Rabung et al., 2009)

Secondary Outcome Measures

change of depressiveness
according to the HEALTH-49 (Rabung et al., 2009)
change of phobic anxiety
according to the HEALTH-49 (Rabung et al., 2009)
change of somatoform complaints
according to the HEALTH-49 (Rabung et al., 2009)
change of mental well-being
according to the HEALTH-49 (Rabung et al., 2009)
change of interactional difficulties
according to the HEALTH-49 (Rabung et al., 2009)
change of self-efficacy
according to the HEALTH-49 (Rabung et al., 2009)
change of activity and participation
according to the HEALTH-49 (Rabung et al., 2009)
change of social support
according to the HEALTH-49 (Rabung et al., 2009)
change of social stress
according to the HEALTH-49 (Rabung et al., 2009)
change of employment prognosis
according to the subjective employment forecast (Mittag et al.,2006)
change of workability
according to the work ability index (Hasselhorn&Freude, 2007)

Full Information

First Posted
July 14, 2021
Last Updated
May 6, 2022
Sponsor
Dr. Becker Hospital Group
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1. Study Identification

Unique Protocol Identification Number
NCT04989842
Brief Title
Effectiveness and Equivalence of an Internet-based Virtual Classroom Intervention for Psychosomatic Aftercare
Official Title
Studies on the Effectiveness and Equivalence of an Internet-based Virtual Classroom Intervention for Psychosomatic Aftercare According to the Hannover Curriculum
Study Type
Interventional

2. Study Status

Record Verification Date
May 2022
Overall Recruitment Status
Completed
Study Start Date
March 1, 2017 (Actual)
Primary Completion Date
December 31, 2021 (Actual)
Study Completion Date
December 31, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Dr. Becker Hospital Group

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Outpatient psychosomatic aftercare after inpatient rehabilitation pursues the goal of helping patients to transfer the achieved rehabilitation result in everyday life and professional life. The Hanover Curriculum has been established as a treatment programme for psychosomatic aftercare. This comprises 25 weekly group sessions and two single therapies at the beginning and at the end of the therapy. In Germany a vast majority of rehabilitants in a psychosomatic rehabilitation clinic has an indication for psychosomatic aftercare, but it is used only by less than half of the patients due to a lack of aftercare therapists. If there is a therapist in the patient's vicinity, there are often long travelling times to the therapist or the patients might feel stigmatized participating in a face-to-face therapy. Thus, the expansion of internet-based aftercare services is recommended. Advantages are that they can be carried out at home, possible cost and time savings and improvement of the care situation. Several meta-analyses provide high evidence for the effectiveness of internet-based therapy offers in depressive and anxiety disorders that are frequent among psychosomatic rehabilitation patients. First randomised controlled studies show that internet-based aftercare services can lead to a symptomatic improvement and to a reduction of relapses. It is currently not clear whether established aftercare concepts, such as the Curriculum Hannover, are also effective in an internet-based format (Curriculum Hannover Online). The present project consists of a superiority study, examining whether participation in Curriculum- Hannover-Online leads to a stronger adoption and maintenance of the health improvements achieved in inpatient rehabilitation in comparison to care as usual, and an equivalnece study, examining, wether the Curriculum Hannover Online is an equivalent treatment option to the existing face-to-face aftercare therapy.
Detailed Description
The use of information and communication technology with the aim of promoting mental health can be described as "e-Mental Health", which is regularly used synonymously with the term "internet-based interventions". With regard to the study situation on internet-based aftercare interventions, especially in Germany, the research is in an early phase. An overview of the possible uses of internet-based treatment approaches in rehabilitation can be found in Lin, Ebert, Lehr, Berking and Baumeister (2013) and - based on the contributions of the Rehabilitation Science Colloquium since 2008 - Baumeister, Lin and Ebert (2013). However, the first randomised controlled studies on aftercare show, in agreement with the studies outlined above, that corresponding offers led to a reduction in relapses compared to Care as Usual (CAU) (Bauer, Okon, Meermann, Kordy, 2013; Ebert, Tarnowski, Gollwitzer, Sieland& Berking, 2013).Both interventions represent new conceptual developments. Regarding the positive findings on the effectiveness of internet-based interventions and with a view to the suboptimal care situation, Kobelt, Winkler and Petermann (2011), for example, recommend the expansion of internet-based aftercare services and their evaluation. The planned project aims to develop an internet-based variant of the aftercare concept Curriculum Hannover (Curriculum-Hannover-Online), to integrate it into routine care and to test its effectiveness. The technology of the virtual classroom is particularly suitable for internet-based interventions providing group therapy (cf. Wolever et al., 2012). For this purpose, the existing manual for Curriculum Hannover (cf. Kobelt et al., 2002) is adapted in the course of the process for the needs of an online intervention. The therapists will be prepared for the specifics of the medium through a train-the-trainer-training for learning how to specifically establish and maintain a therapeutic relationship between therapist and participants. It is assumed that this new program for outpatient aftercare after inpatient psychosomatic rehabilitation can be an effective and useful therpy for patients who do not have access to the existing face-to-face aftercare therapies.. The Virtual Classroom is a direct, video- or audio-synchronous and multimedia contact between therapist and patient. The main question of the superiority study is: A. Does participation in the Curriculum-Hannover-Online lead to improved uptake and maintenance of the health improvements achieved in inpatient rehabilitation? B. Can the implementation of the Curriculum-Hannover-Online be designed in such a way that its use as a routine procedure in rehabilitation can be recommended? C. Can the Curriculum-Hannover-Online be accepted by the relevant stakeholders to the same extent as the face-to-face version of the Curriculum-Hannover-Online? For the successful introduction of a new treatment approach, in addition to the proof of its effectiveness, significant challenges have to be overcome with regard to the organisation of work processes, the involvement of all actors involved in the process (especially patients, practitioners, management). The main question of the equivalence study is: A.Does participation in the Curriculum-Hannover-Online lead to an equivalent adoption and maintenance of the health improvements achieved in inpatient rehabilitation? B. Can the implementation of the Curriculum-Hannover-Online in addition to the offer of the face-to-face variant be designed in such a way that its use as a rou- tine procedure in rehabilitation can be recommended? C.Can the Curriculum-Hannover-Online be accepted by the relevant stakeholders to the same extent as the face-to-face version of the Curriculum-Hannover-Online? D.Can characteristics be identified that allow a differential indication for the recommendation to participate in the Curriculum Hannover in its online or face-to-face variant? E.What are the additional advantages of the Curriculum Hannover Online from the perspective of patients, therapists, service providers and health care providers? Both studies will be conducted as two-arm randomised controlled trials. Individual rehabilitation patients will be randomised to the respective study arms. The system is based on a randomisation list (permuted blocks of variable length) with the help of the "Randlist" software at the sites. The order of the completed questionnaires determines the position in the list. All data of the participants will be treated in accordance with the data security regulations (DSGVO), good scientific practice and the ethical requirements. Furthermore, all patients are informed about the project, ethics and data protection in a generally understandable way by a cover letter from their clinic before the treatment. All project staff are obliged to comply with the ethics guidelines and to maintain confidentiality. The pre- and post-data of the patients are combined by means of a personal code, which does not allow any conclusion about the participant.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Psychosomatic Disorder, Mental Disorder
Keywords
Rehabilitation, Psychosomatics, Aftercare, webbased aftercare therapy

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
6023 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Intervention group 1
Arm Type
Active Comparator
Arm Description
webbased aftercare
Arm Title
Control group
Arm Type
No Intervention
Arm Description
care as usual
Arm Title
Intervention group 2
Arm Type
Active Comparator
Arm Description
webbased aftercare
Arm Title
face-to-face aftercare
Arm Type
Active Comparator
Arm Description
face-to-face aftercare
Intervention Type
Behavioral
Intervention Name(s)
Curriculum Hannover
Intervention Description
The methodology uses a natural variation design within the Dr. Becker Clinical Group. The interventions consist of a face-to-face or a digital psychosomatic aftercare basing upon the concept of the Curriculum Hanover. A control group is included that does not receive these two interventions (but receives a similar rehabilitation treatment to the intervention groups).
Primary Outcome Measure Information:
Title
change of psychic and somatoform complaints
Description
according to the HEALTH-49 (Rabung et al., 2009)
Time Frame
up to 18 months
Secondary Outcome Measure Information:
Title
change of depressiveness
Description
according to the HEALTH-49 (Rabung et al., 2009)
Time Frame
up to 18 months
Title
change of phobic anxiety
Description
according to the HEALTH-49 (Rabung et al., 2009)
Time Frame
up to 18 months
Title
change of somatoform complaints
Description
according to the HEALTH-49 (Rabung et al., 2009)
Time Frame
up to 18 months
Title
change of mental well-being
Description
according to the HEALTH-49 (Rabung et al., 2009)
Time Frame
up to 18 months
Title
change of interactional difficulties
Description
according to the HEALTH-49 (Rabung et al., 2009)
Time Frame
up to 18 months
Title
change of self-efficacy
Description
according to the HEALTH-49 (Rabung et al., 2009)
Time Frame
up to 18 months
Title
change of activity and participation
Description
according to the HEALTH-49 (Rabung et al., 2009)
Time Frame
up to 18 months
Title
change of social support
Description
according to the HEALTH-49 (Rabung et al., 2009)
Time Frame
up to 18 months
Title
change of social stress
Description
according to the HEALTH-49 (Rabung et al., 2009)
Time Frame
up to 18 months
Title
change of employment prognosis
Description
according to the subjective employment forecast (Mittag et al.,2006)
Time Frame
up to 18 months
Title
change of workability
Description
according to the work ability index (Hasselhorn&Freude, 2007)
Time Frame
up to 18 months

10. Eligibility

Sex
All
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Patients after psychosomatic rehabilitation indication for outpatient psychosomatic aftercare are included in both studies. access to a standard PC and broadband internet connection is required (DSL or LTE). Exclusion Criteria: Persons who are are discharged with a capacity of less than three hours per day on the general labour market, receive or have applied for a pension of at least two-thirds of the full pension, receive a benefit that is regularly paid until the start of an old-age pension. suffering from acute addiction disorder / acute psychosis
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Alina Dahmen, MD
Organizational Affiliation
Dr. Becker Hospital Group
Official's Role
Study Director
Facility Information:
Facility Name
Dr. Becker Hospital Group
City
Cologne
ZIP/Postal Code
50968
Country
Germany

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
Individual participant data (IPD) will not be published. Other researchers are welcome to get in contact with the PI to get access to anonymous data.
Citations:
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25273302
Citation
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Effectiveness and Equivalence of an Internet-based Virtual Classroom Intervention for Psychosomatic Aftercare

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