Who is eligible for clinical trial NCT06374537?

Participants must meet the protocol's inclusion criteria for Frailty. The stated age range is 18 Years. Confirm all requirements with the study coordinator.

Does clinical trial NCT06374537 provide travel or cost reimbursement?

Check with the site coordinator at the participating facility for travel and lodging stipend availability, and for which routine-care costs are covered.

🏛️ Verified NIH Record • Updated 2025-08-12

Evaluate the Impact of Targeted Physical Activity on Clinically Debilitated Dialysis Patients. (NCT06374537)

Evaluating the Impact of Targeted Physical Activity on Clinically Debilitated Dialysis Patients.

🟢 Recruiting Observational / Diagnostic 📋 Clinical Research Protocol Sponsor: University of Illinois at Chicago

🩺 Plain-English Summary (8th-Grade Level)

This research is being done to better understand the impact of the use of a specific physical activity training program (GH Method) in dialysis/kidney disease patients.

Who can join: To join this study, participants generally need to meet the listed inclusion criteria (2 items) and avoid the listed exclusions (4 items).

Location: University of Illinois at Chicago — Chicago, Illinois

Age range: 18 Years

🧪 Interventions in This Study

Muscle Therapy (OTHER)

📋 "Do I Qualify?" — 1-Minute Self Screener

Instant Checklist

Check every box below. If you can check all of them, you may meet the study's basic screening requirements (final eligibility is confirmed by the site team).

Clinically debilitated patients, currently on dialysis, or have CKD 4 (GFR between 15 and 29), or have CKD 5 (GFR below 15), or post- kidney transplant (for PPKT Subgroup only) as stated by patient's health care professional.
Adequate cognitive ability to complete the questionnaires, give consent for the study and follow the physical and diet instructions

Usually NOT eligible if any of the following apply:

Exclusion Criteria:
cardiac/pulmonary disease that contraindicate the physical training
Unable to give consent
Unable to travel to the training center

🔍 Extracted verbatim from the official NIH eligibility criteria. Always confirm with the study coordinator.

📍 All Participating Trial Locations (1 Sites)

University of Illinois at Chicago — Chicago, Illinois

📞 Contact the Study Coordinator

Phone: (312) 996-9594

Email: isanti@uic.edu

Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.

💰 Cost, Insurance & Patient Rights

100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
Voluntary Participation: You may withdraw at any time without affecting your standard medical care.

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Safety of Cultured Allogeneic Adult Umbilical Cord Derived Mesenchymal Stem Cell Intravenous Infusion for Aging Frailty — St John's,
Frailty Rehabilitation — Hamilton, Ontario
High Intensity Interval Training (HIIT) to Reduce Frailty and Enhance Resilience in Older Veterans — Kansas City, Missouri
Meal Delivery and Exercise — Houston, Texas
SCM Muscle as a Marker for Frailty in Patients Undergoing ENT Surgery — New York, New York

Explore by condition: All Frailty clinical trials

💡 How to Participate

Check the checklist above to see if you may qualify.
Contact the study coordinator using the phone/email above.
Ask about the visit schedule, what is covered at no cost, and any travel support.
Confirm with your own doctor before making a decision.

🏛️ View Official NIH Record ↗