Trials / Recruiting
RecruitingNCT06699446
The "Seamless" Patient:From Preoperative Preparation to Postoperative Rehabilitation
The "Seamless" Patient: From Preoperative Preparation to Postoperative Rehabilitation
- Status
- Recruiting
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 300 (estimated)
- Sponsor
- Hannover Medical School · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The "seamless" patient: from preoperative preparation to postoperative rehabilitation. The effects of digital services for perioperative care of patients undergoing cardiac surgery will be investigated
Detailed description
Intervention by randomization in: G1. "Standard of care" Previous postal call-in without additional communication or special follow-up G2: Intensified patient education via classical communication channels as well as provision of information material for outpatient, preoperative pre-rehabilitation (respiratory training, exercise therapy). Establish an individualized rehabilitation plan and telephone postoperative communication (postoperative for Patient-Reported Experience Measures (PREMs) and Patient-Reported Outcome Measures (PROM) analysis) with the surgical center. G3: Intensified education on new media (mobile app) with outpatient preoperative rehabilitation (respiratory training, exercise therapy). Creation of an individualized rehabilitation plan and postoperative, two-way communication via mobileapp. This project combines the establishment of outpatient pre-rehabilitation with the additional benefit of interrogating patient-reported outcome (PROs) with individualized rehabilitation. Through the improved exchange of information and the resulting more intensive care of patients alone, we hope not only to improve the quality of life, but also to reduce postoperative mortality and morbidity. The use of new techniques with the establishment of a mobile-based app should provide a decisive advantage in the effectiveness of the measures in this regard. The integration of secure, direct, and always-available communication channels will both improve the flow of information and enhance patients' sense of security in an increasingly fast-moving healthcare system. Hypotheses: * The intervention in G2 "classic forms of communication" does not significantly improve the primary and secondary endpoints compared to the control group G1. * The intervention in G3 "next level" communication via app leads to a significant improvement of the primary and secondary endpoints compared to control group G1. * The rate of exercise performance (in the prehabilitation and rehabilitation phases; % of days) is significantly higher in the G3 "next level" communication via app group compared to the G2 "classical forms of communication" group. * Intervention in G2 "classical forms of communication" and G3 "next level" communication via app leads to significant improvement in PREMs compared to control group G1. * The questionaires: EQ-VAS, PROMIS-10 and HSSI are equally suitable for mapping the health status of patients\* in the postoperative course. * The feedback rate (completion of the query) on health status is significantly higher for the questionaires EQ-VAS compared to questionaire PROMIS-10, questionaire HSSI and questionaire MLHFQ. * In patients\* who develop postoperative pericardial tamponade, pneumonia, or surgical access wound complication (bleeding/Dressler syndrome, infection/sepsis, wound dehiscence/infection, mechanical instability), Questionaire EQ-VAS scores drop significantly before diagnosis. The questionaire EQ-VAS is therefore suitable as a non-specific postoperative parameter for triggering early further diagnostics.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | pre rehabilitation | preoperative pre-rehabilitation (respiratory training, exercise therapy). Establish an individualized rehabilitation plan and postoperative communication via telephone or app |
Timeline
- Start date
- 2023-06-28
- Primary completion
- 2026-06-01
- Completion
- 2026-12-01
- First posted
- 2024-11-21
- Last updated
- 2024-11-21
Locations
1 site across 1 country: Germany
Source: ClinicalTrials.gov record NCT06699446. Inclusion in this directory is not an endorsement.