Actively Recruiting

Phase Not Applicable
Age: 13Years - 18Years
All Genders
NCT06642246

Sleep Promotion and Pediatric Hypertension

Led by Children's Hospital of Philadelphia · Updated on 2026-02-18

10

Participants Needed

1

Research Sites

15 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Determine the effectiveness and feasibility of a mobile health sleep extension approach in the pediatric nephrology setting, to increase sleep duration and reduce systolic and diastolic blood pressure.

CONDITIONS

Official Title

Sleep Promotion and Pediatric Hypertension

Who Can Participate

Age: 13Years - 18Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Speak, read, and write in English.
  • Parental or guardian permission and child assent.
  • Have access to a computer, tablet, or smartphone with internet or data plan.
  • Sleep duration on school nights is 7.5 hours or less as reported by parent.
  • Recently diagnosed with essential hypertension confirmed by ambulatory blood pressure monitoring.
  • Willing to stop over-the-counter sleep aids during the study if currently using them.
  • Parent or guardian of an eligible child enrolled in the study and able to speak, read, and write in English.
Not Eligible

You will not qualify if you...

  • Clinical diagnosis of any sleep disorder (e.g., sleep apnea) or regular use of prescribed sleep aids.
  • Chronic medical conditions lasting longer than 3 months that require regular medication.
  • Use of medications that affect blood pressure such as anti-hypertensive drugs, glucocorticoids, or stimulants.
  • Diagnoses associated with high blood pressure like cardiac disease, kidney disease, or diabetes.
  • Parents or guardians with limited English proficiency.

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Children's Hospital of Philadelphia

Philadelphia, Pennsylvania, United States, 19146

Actively Recruiting

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Research Team

J

Jonathan Mitchell

CONTACT

A

Abby Salem

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

OTHER

Number of Arms

1

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