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Data Sharing as a Challenge for the Response Rate in Health Care Research in Germany? Randomized-controlled Study to Examine the Impact of Different Data Sharing Statements on the Response Rate

Data Sharing as a Challenge for the Response Rate in Health Care Research in Germany? Randomized-controlled Study to Examine the Impact of Different Data Sharing Statements on the Response Rate

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00013115
Enrollment
536
Registered
2017-10-18
Start date
2017-12-12
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Willingness to participate in the study depending on the data sharing statement F31 F32 F33 F34.1 F40 F41 F43.2 F45 F10 F20 G35

Interventions

Group 1: Participants in the intervention group (IG-ADÖ) receive the following section on the publication of data in the informed consent sheet: "Scientific publications are made in an anonymous form

Sponsors

Universitätsklinikum Hamburg-Eppendorf
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: - insured by the AOK BW - at least 18 years old - treated by a practitioner or therapist with admission in Baden-Wuerttemberg, Germany - are on sick leave due to a mental or neurological disorder (bipolar disorder, depressive disorder, anxiety disorder, adaptation disorder, somatoform disorder, alcohol abuse disorder, schizophrenia, multiple sclerosis) at the first time in the last 12 month

Exclusion criteria

Exclusion criteria: - have a guardian - were on sick leave due to a mental disorder or multiple sclerosis during the least year

Design outcomes

Primary

MeasureTime frame
Willingness to participate in the PNP evaluation study is operationalized by the return of informed consent for participation in the study

Secondary

MeasureTime frame
Actual participation in the PNP evaluation study is operationalized by the return of t0 questionnaire sent at baseline (short-term participation) and return of t1 questionnaire sent 12 month after baseline (long-term participation)

Countries

Germany

Contacts

Public ContactJulia Magaard

Zentrum für Psychosoziale Medizin, Institut und Poliklinik für Medizinische Psychologie, Universitätsklinikum Hamburg-Eppendorf

j.magaard@uke.de040 / 7410-56683

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Aug 9, 2026