Analysis of Frailty Syndrome Within the Framework of the Innovation Fund Project PRÄP-GO (ANA-PRÄP-GO)
Brief Summary
The patients included in PRÄP-GO and the corresponding comparison cohorts will be offered to participate in this complementary study in order to be able to carry out a detailed characterization and phenotyping of the frailty complex. Amendment vote of 08/05/2024: Recruitment extension of Non-frail surgical control group (NFC cohort) until August 31, 2025.
Detailed Description
As part of the innovation fund project PRÄP-GO (EA1/225/19), a multimodal intervention is being conducted in patients with a frailty syndrome. However, the health care research project is limited to evaluating clinical issues only. In order to be able to research further pathophysiological, clinical, psychosocial and work-organizational connections, different groups of participants will be offered the participation in this scientific support program of PRÄP-GO. The groups of participants in this accompanying program ANA-PRÄP-GO are: * Randomized study patients with a frailty syndrome of the intervention study PRÄP-GO (PG cohort) * Non-frail surgical control group (NFC cohort) * Non-surgical comparison group (NO cohort) * Participants with health professions (GB cohort) Additionally, relatives of the patients can be included. Subprojects are included to reflect research questions of interest in sub groups: * Success of endoprosthetic implants (clinical outcome and gait pattern after total hip arthroplasty and total knee arthroplasty in frail patients) * Functional treatment outcome and health-related quality of life after elective spinal surgery in the PG cohort, in the NFC cohort, and in the NO cohort * Hemodynamic evaluation in patients of the PG and NFC cohort with preoperative abnormal cardiovascular function * Establishment of a German standard database for 14 CANTAB tests by CANTAB Connect technology * Aggregated evaluation of the cognitive data of different surgical cohorts from studies carried out at the department of anesthesiology to describe domain-specific changes in the perioperative course * Perspectives of different health professional groups regarding barriers and facilitators in the implementation of a prehabilitation program and necessary changes in skill, organizational and management, and communication in an interdisciplinary setting * Perspectives of patients and significant others regarding the organizational pathway of the prehabilitation program * Frequency, pathophysiology and trajectory of muscle weakness as well as functional impairments of patients admitted to intensive care units of the PG and NFC cohort and their long-term outcomes. * The gut microbiome as a potential risk factor for perioperative neurocognitive disorders (PNDs) in the elderly * Evaluation of nutrition data in all cohorts (e.g. adherence to mediterranean diet, nutrition habits, nutritional status, dental status etc.)
Interventions
Primary Outcomes
Trial Information
NCT04880824
Completed
OBSERVATIONAL
Charite University, Berlin, Germany
December 15, 2025