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Prehabilitation for Kidney Transplant Candidates
NCT06886256 · View on ClinicalTrials.gov ↗
Study Summary
This interventional trial seeks to determine the feasibility of wearable sensors to provide data from patients while undergoing supervised exercise.
Conditions Studied
Interventions
- DEVICE Empatica EmbracePlus
- DEVICE Polar H10 Heart Rate Monitor
- DEVICE Apple Watch Ultra 2
Study Locations (1)
Texas
- Houston Methodist Hospital System — Houston
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 15 participants |
| Start Date | 2025-03-26 |
| Est. Completion | 2025-09-30 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06886256
The ClinicalTrials.gov registry entry for NCT06886256 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 15 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is The Methodist Hospital Research Institute, which has 203 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 3 conditions, with Frailty appearing as the primary indexed condition, and to 3 interventions — of which Empatica EmbracePlus is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT06886256 reports 1 study location spanning 1 distinct geographic area — top geographies include Texas. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT06886256 about?
NCT06886256 is a clinical study titled "Prehabilitation for Kidney Transplant Candidates". This interventional trial seeks to determine the feasibility of wearable sensors to provide data from patients while undergoing supervised exercise.
What is the current status of trial NCT06886256?
This trial is currently recruiting. It is a NA study. The enrollment target is 15 participants. The study started on 2025-03-26. Estimated completion is 2025-09-30.
What conditions does trial NCT06886256 study?
This clinical trial studies the following conditions: Frailty, Kidney Transplantation, Chronic Kidney Insufficiency. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT06886256?
The interventions under investigation include: Empatica EmbracePlus (DEVICE), Polar H10 Heart Rate Monitor (DEVICE), Apple Watch Ultra 2 (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06886256?
This trial is sponsored by The Methodist Hospital Research Institute, which has 203 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT06886256 being conducted?
This trial has 1 study location across Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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