Using routine clinical data to improve rehabilitation for people with disabilities and chronic diseases
Rehablines: a Further Use Databank to (re)Use Routine Clinical Data for Scientific Research in Rehabilitation of People With Physical Disabilities and/or Chronic Diseases
This study looks at using regular health data from patients with disabilities and chronic diseases to see how rehabilitation treatments can be improved and personalized for better care.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 20000 (estimated) |
| Sex | All |
| Sponsor | University Medical Center Groningen Academic / other |
| Locations | 1 site (Groningen) |
| Trial ID | NCT06750601 on ClinicalTrials.gov |
What this trial studies
This initiative aims to collect and utilize routine clinical data from patients receiving treatment at the Center for Rehabilitation at the University Medical Center Groningen. The data will be organized into a databank to facilitate high-quality scientific research focused on patient characteristics, disease processes, and treatment outcomes. By analyzing this data, the project seeks to provide insights into the effectiveness of rehabilitation treatments and personalize care based on comparisons with a larger patient population. The approach emphasizes the efficient use of existing data to enhance future rehabilitation practices.
Who should consider this trial
Good fit: Ideal candidates for this initiative are individuals receiving care at the Center for Rehabilitation of the University Medical Center Groningen.
Not a fit: Patients not receiving treatment at the Center for Rehabilitation may not benefit from this initiative.
Why it matters
Potential benefit: If successful, this could lead to more personalized and effective rehabilitation treatments for patients with physical disabilities and chronic diseases.
How similar studies have performed: Other studies utilizing routine clinical data for rehabilitation research have shown promise, indicating that this approach could be beneficial.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * all participants receiving care at the Center for Rehabilitation of the University Medical Center Groningen Exclusion Criteria: * n.a.
Where this trial is running
Groningen
- Center for Rehabilitation of the University Medical Center Groningen — Groningen, Netherlands (Recruiting)
Study contacts
- Study coordinator: K van Kammen, PhD, PhD
- Email: rehablines@umcg.nl
- Phone: +3150 - 361 6160
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.