RECRUITING

Sensor-based Congestion ALert for Events in Peritoneal Dialysis (SCALE-PD)

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

Sensor-based Congestion Alert for Events in Peritoneal Dialysis (SCALE-PD)

Quick Facts

Study Start:2025-07
Study Completion:2026-06
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT07059962

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:21 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. 1. Age 21 years or older
  2. 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. 3. Able to stand on two bare feet unassisted
  4. 4. Receiving automated peritoneal dialysis for the treatment of ESKD
  5. 5. Followed on the Vantive Sharesource Remote Patient Management Platform
  1. 1. Undergoing or plan to undergo hemodialysis in the next 12 months
  2. 2. Have a life expectancy of less than 12 months
  3. 3. Are pregnant or plan to become pregnant during the next 12 months
  4. 4. Weigh greater than 375 lbs
  5. 5. Planned kidney transplant within the next 12 months
  6. 6. Have an implanted neurostimulator system

Contacts and Locations

Study Contact

Corey Centen
CONTACT
415-990-5415
corey@bodyport.com
Dorothy Kwok
CONTACT
669-240-3077
dorothy@bodyport.com

Study Locations (Sites)

aQua Research Institute, LLC
Houston, Texas, 77058
United States

Collaborators and Investigators

Sponsor: Bodyport Inc.

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2025-07
Study Completion Date2026-06

Study Record Updates

Study Start Date2025-07
Study Completion Date2026-06

Terms related to this study

Keywords Provided by Researchers

  • kidney disease
  • peritoneal dialysis
  • fluid overload
  • heart failure

Additional Relevant MeSH Terms

  • Kidney Disease
  • Peritoneal Dialysis (PD)
  • End Stage Kidney Disease (ESRD)