Skip to content

Sepsis survivors Monitoring and coordination in Outpatient Health care

Sepsis survivors Monitoring and coordination in Outpatient Health care - Smooth

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00000741
Enrollment
290
Registered
2011-03-02
Start date
2011-02-28
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

A41

Interventions

Group 1: control group: usual care Group 2: Patients of the intervention group will receive for 12 month in total a specific Disease Management Program, consisting of discharge management, patient mon

Sponsors

Center for Sepsis Control & Care, Universitätsklinikum Jena
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: - Survivors of severe sepsis or septic shock (ICD-10: A41) - at least two SIRS criteria - at least one organ dysfunction - Adults - sufficient German language skills - Patients have primary care provider

Exclusion criteria

Exclusion criteria: - Dementia (TICSM < 27) - guardianship before sepsis - nursing home residents - severe language/speech disorder - deaf or blind patients - insufficiant German language skills

Design outcomes

Primary

MeasureTime frame
Health related quality of life / Physical Health Summary Scale (SF-36 – Patient survey) after 6 months

Secondary

MeasureTime frame
6, 12 and 24 month after ICU discharge: - Health related quality of life / Physical Health Summary Scale (SF-36 – Patient survey) - Patient adherence (Moriskey – Patient survey) - Process of care (PACIC (Patient Assessment of Care for Chronic Conditions)- Patient survey) - Death for any reason - Number of readmissions for any reason - Number of hospital days for any reason (GP/ post-sepsis-center documentation) - Numbers of contacts to GP (GP documentation) - Numbers of contacts to specialists (GP documentation) - Days on which patient is unfit to work (GP documentation) Medication (PZN and modus – Patient survey / GP/ post-sepsis-center documentation) - cognitive function (TICS-M (Telephone Interview of Cognitive Status)- Patient survey) - nutritional status (MUST (Malnutrition Universal Screening Tool-GP documentation and (Patient survey) - chronic pain (GCPS (Graded Chronic Pain Scale) - Patient survey) - neuropathic symptoms (NSS (Neuropathie-Symptom Score)- Patient survey) - posttraumatic stress syndrom symptoms (PTSS-10 (Post-Traumatic Stress Syndrome 10-Questions Inventory - Patient survey) - depressive symptoms (MDI (Major Depression Inventory)- Patient survey) - Insomnia symptoms (RIS (Regensburger Insomniebogen)- Patient survey) - ADL (instrumental) activities of daily life (Patient survey) - smelling, hearing, degustation disfunction (Patient survey) - medication use/addiction (KFM (Kurzfragebogen zum Medikamentengebrauch)- Patient survey) - pension/retirement approval all but month 6: - Physical activity (XSMFA-D - Patient survey) month 12 only: - body perception (DKB (Dresdner Körperfragenbogen) - Patient survey) - Attachment pattern (ECR-S (Experiences in Close Relationsship Scale Short form)

Countries

Germany

Contacts

Public ContactKonrad Schmidt

Institut für AllgemeinmedizinUniversitätsklinikum Jena, Friedrich-Schiller-Universität

konrad.schmidt@med.uni-jena.de; konrad.schmidt@charite.de++49 (0) 3641 9395800

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Mar 20, 2026