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Sensor-based Congestion ALert for Events in Peritoneal Dialysis (SCALE-PD)
RecruitingObservational study
Sensor-based Congestion Alert for Events in Peritoneal Dialysis (SCALE-PD)
Who can join
Ages 21 and older · All sexes
Full eligibility criteria
Inclusion Criteria: 1. Age 21 years or older 2. Able to speak and read English, or able to speak and read Spanish and has a caregiver or family member who speaks English and can provide assistance 3. Able to stand on two bare feet unassisted 4. Receiving automated peritoneal dialysis for the treatment of ESKD 5. Followed on the Vantive Sharesource Remote Patient Management Platform Exclusion Criteria: 1. Undergoing or plan to undergo hemodialysis in the next 12 months 2. Have a life expectancy of less than 12 months 3. Are pregnant or plan to become pregnant during the next 12 months 4. Weigh greater than 375 lbs 5. Planned kidney transplant within the next 12 months 6. Have an implanted neurostimulator system
About the study
To explore the use of the Bodyport Cardiac Scale in predicting worsening of events due to fluid overload in patients with kidney disease on peritoneal dialysis.
What is being tested
- Bodyport Cardiac Scale (device)
Sponsor: Bodyport Inc. · Participants: 125 · Started: Sep 9, 2025
Contact the study team
- Corey Centen · Phone: 415-990-5415
- Dorothy Kwok · Phone: 669-240-3077
Official record on ClinicalTrials.gov — NCT07059962
Locations in the U.S.
| California | Desert Cities Dialysis, Victorville |
| Georgia | Southeastern Clinical Research Institute, Augusta |
| Illinois | Northwestern University, Chicago |
Conditions
From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.