Improving recovery for elderly patients after trauma
Optimized Recovery After Trauma in Geriatric Patient (Gero - ERAT)
This study is testing a new care approach to help older patients recover better and faster after experiencing trauma.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 540 (estimated) |
| Ages | 65 Years and up |
| Sex | All |
| Sponsor | Vastra Gotaland Region Government |
| Locations | 1 site (Gothenburg) |
| Trial ID | NCT04092504 on ClinicalTrials.gov |
What this trial studies
This project investigates a new care concept called Geriatric Enhanced Recovery After Trauma (gero-ERAT) that combines structured care approaches to enhance recovery for elderly patients who have experienced physical trauma. The study aims to implement and evaluate this care model at the trauma care unit of Sahlgrenska University Hospital. It includes qualitative interviews to gather insights on patient experiences during recovery, with the goal of reducing complications, shortening care times, and minimizing hospital readmissions. The overarching aim is to improve the quality of life for elderly patients and reduce healthcare costs.
Who should consider this trial
Good fit: Ideal candidates for this study are individuals aged 65 and older who are hospitalized due to physical trauma and can communicate in Swedish.
Not a fit: Patients receiving palliative care or those with cognitive impairments may not benefit from this study.
Why it matters
Potential benefit: If successful, this approach could significantly enhance recovery outcomes and quality of life for elderly trauma patients.
How similar studies have performed: Previous studies have shown promise in using structured care models for improving recovery outcomes in surgical contexts, making this approach both relevant and potentially impactful.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * ≥ 65 years old * In hospital due to physical trauma * Able to speak and understand Swedish Exclusion Criteria: * Documented palliative care * Cognitive impairment
Where this trial is running
Gothenburg
- Sahlgrenska university hospital — Gothenburg, Sweden (Recruiting)
Study contacts
- Principal investigator: My Engström, PhD — Sahlgrenska University Hospital, Department of Surgery.
- Study coordinator: My Engstrom, PhD
- Email: my.engstrom@vgregion.se
- Phone: + 46 (31) 3428404
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.