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Implementation of the Internet-based Aftercare Program 'GSA-Online Plus'

Implementation of the Online Aftercare Intervention 'GSA-Online Plus' (Healthy and Without Stress at the Workplace)

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03019718
Enrollment
88
Registered
2017-01-13
Start date
2016-07-31
Completion date
2017-10-31
Last updated
2018-03-05

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

Conditions

Implementation

Keywords

Inpatient rehabilitation, Internet-based intervention, Aftercare, Return to work, Psychodynamic

Brief summary

The purpose of this study is to implement the internet-based aftercare program 'GSA-Online plus' in several rehabilitation clinics with patients of different indications (psychosomatic, orthopedic and cardiovascular diseases). 'GSA-Online plus' is an internet-based aftercare program for patients with work-related problems or anxieties facing return to work after longterm sickness absence and inpatient rehabilitation. The patients have access to various exploratory and motivational videos on the study website until their inpatient rehabilitation ends. Afterwards, they start a 12-week writing intervention based on a psychotherapeutic concept, the psychodynamic 'Core Conflictual Relationship Theme Method (CCRT)'. Patients write weekly online diary entries which are answered by anonymous online therapists usually within 24 hours. In a previous randomised controlled trial the efficacy of the intervention was determined, whereas the current study focuses on the implementation and realization in a naturalistic setting (effectiveness).

Interventions

OTHERGSA-Online plus

A 12-week online writing intervention based on the Core Conflictual Relationship Theme Method (CCRT) with feedback provided by online therapists.

Sponsors

Deutsche Rentenversicherung
CollaboratorOTHER
Koblenz University of Applied Science
CollaboratorOTHER
Johannes Gutenberg University Mainz
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Referral (physician) or request (patient) to take part in the internet-based aftercare program * Current or prospective employment within 4 weeks after inpatient rehabilitation * Private internet access * Informed consent * Knowledge of the German language

Exclusion criteria

* Severe psychiatric or somatic disease

Design outcomes

Primary

MeasureTime frameDescription
Recommendation rate of 'GSA-Online plus'study inclusion (T1)How often will 'GSA-Online plus' be recommended as an aftercare after inpatient rehabilitation?
Number of patients participating in 'GSA-Online plus'12 weeks after study inclusion (T14)At least 66% of patients with a corresponding recommendation should use 'GSA-Online plus' at least once.

Secondary

MeasureTime frameDescription
Willingness to pay12 weeks after study inclusion (T14)Self developed items if and how much money participants would pay for GSA-Online+
Working ability measured with the short form of the Work Ability Index (WAI)At study inclusion (T1) and 12 weeks later (T14)
Depressive symptoms measured with a subscale of the Patient Health Questionnaire (PHQ-9)At study inclusion (T1) and 12 weeks later (T14)
Anxiety measured with the General Anxiety Disorder Scale (GAD-7)At study inclusion (T1) and 12 weeks later (T14)
Somatic symptom burden measured with the Somatic Symptom Scale-8 (SSS-8)At study inclusion (T1) and 12 weeks later (T14)
Psychosocial stressors measured with a subscale of the Patient Health Questionnaire (PHQ-10)At study inclusion (T1) and 12 weeks later (T14)
Overall health status measured with the EQ-5D-3L questionnaireAt study inclusion (T1) and 12 weeks later (T14)
Evaluation of GSA-Online+12 weeks after study inclusion (T14)Self developed items to assess overall satisfaction with, helpfulness and utilization of GSA-Online+
Loneliness measured with the Loneliness Scale (LS-S)At study inclusion (T1) and 12 weeks later (T14)
Psychological stress measured with the Perceived Stress Scale (PSS-4)At study inclusion (T1) and 12 weeks later (T14)
Personal resources measured with the Oslo Support Scale (OSS-3)At study inclusion (T1) and 12 weeks later (T14)
Personal resources measured with the Brief Resilient Coping Scale (BRCS)At study inclusion (T1) and 12 weeks later (T14)
Regular Monitoring of self-rated health statusup to 12 weeks from study inclusion (T2-T13)Item drawn from the EQ-5D-3L questionnaire
Regular Monitoring of self-rated work abilityup to 12 weeks from study inclusion (T2-T13)Item drawn from the Work Ability Index (WAI)
Evaluation of the therapeutic feedbackup to 12 weeks from study inclusion (T2-T13)Two self developed items ('How satisfied are you with ... / How helpful was therapeutic feedback') on a five-point Likert scale.
General capability measured with the Sheehan-Disability ScaleAt study inclusion (T1) and 12 weeks later (T14)
Future prospects of employment measured with the Subjective Prognosis of Work Ability Scale (SPE)At study inclusion (T1) and 12 weeks later (T14)

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 24, 2026