Using routine clinical data to improve rehabilitation for people with disabilities and chronic diseases

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

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.

Why it matters

Who can join: the full rules

Inclusion Criteria:

* all participants receiving care at the Center for Rehabilitation of the University Medical Center Groningen

Exclusion Criteria:

* n.a.

Where it's running

• 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

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.