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Conception, implementation and feasibility of a study about the evaluation of a web-based post-rehabilitation support (website) for different medical indications – at first for patients with adiposity and/or diabetes type 2.

Conception, implementation and feasibility of a study about the evaluation of a web-based post-rehabilitation support (website) for different medical indications – at first for patients with adiposity and/or diabetes type 2.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00008880
Enrollment
100
Registered
2015-07-24
Start date
2016-01-01
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

E66 E11

Interventions

Group 1: Interviews with experts and patients about the demands and needs of assistance during a post-rehabilitation support. Patients are surveyed about needs of assistance during a post-rehabilitati

Sponsors

Institut für Rehabilitationsforschung Norderney
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients who completed a stationary rehabilitation in Klinik Rosenberg • with main diagnosis adiposity or diabetes type 2 • with technical and cognitive requirements to use the internet • who sign the declaration of agreement to participate in the study • who have sufficient knowledge in the German language (in particular in writing)

Exclusion criteria

Exclusion criteria: • status after bariatric surgery • severe psychiatric disorder (e.g. at risk of suicide, severe eating disorder) • severe somatic disease (cancer, status after LTX), that has a greater impact on the prediction of the patient than the metabolism disease

Design outcomes

Primary

MeasureTime frame
The post-rehabilitation support (website) is available and is prepared to be used by patients in Klinik Rosenberg with adiposity and/or diabetes type 2. In addition we compare how control group and intervention group achieved their aims after 3 month. The attainment of the aims is estimated by the patients using a scale with 10 stages. In this pilot study we don´t anticipate a significant difference, but we want to estimate the expected effect of the intervention on the attainment of the aims. This is important to calculate the necessary number of cases of the evaluation study.

Secondary

MeasureTime frame
body weight after 3 months, HbA1c after 3 months

Countries

Germany

Contacts

Public ContactHarald Fischer

Klinik Rosenberg der DRV Westfalen

harald.fischer@drv-westfalen.de05253 970 525

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026