Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT07049783 · ClinicalTrials.gov registry record · NA

Examining the Circadian Timing Effects of the Hypotensive Response to Exercise

A NA study of Hypertension and Circadian Rhythm, sponsored by Freda Patterson.

Recruiting
Registry status
NA
Development phase
30
Enrollment target
1
Study location

NCT07049783: Recruiting NA study of Hypertension and Circadian Rhythm, sponsored by Freda Patterson.

NCT07049783 is a NA study of Hypertension and Circadian Rhythm that is actively recruiting participants, run by Freda Patterson. The registered enrollment target is 30 participants, below the 3,507-participant average among 470 other Hypertension trials with a reported enrollment target (99% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT07049783, a NA study of Hypertension and Circadian Rhythm, is actively recruiting participants, sponsored by Freda Patterson.

RECRUITING
Registry status
NA
Development phase
30 participants
Enrollment target
1
Study location

Study Summary

The goal of this study is to learn how exercise timing affects blood pressure in adults with elevated or high blood pressure. Exercise can influence the body's natural 24-hour rhythms, including blood pressure patterns. A single exercise session can lower blood pressure for up to 24 hours, but it is not fully understood how the time-of-day for exercise affects this response. The main question this study aims to answer is: • When the same participant exercises at different times of day (morning, afternoon, or evening), how does this affect the participant's blood pressure over the next 24 hours? Participants will: * Undergo an in-lab assessment of individual biological rhythm that will indicate the clock-time for an individual's biological night * Complete 3 supervised treadmill exercise sessions * 1 in the biological morning (biological night + 10 hours) * 1 in the biological afternoon (biological night + 15 hours) * 1 in the biological evening (biological night + 20 hours) * Complete a 24-hour blood pressure assessment before and after each exercise session

Primary Outcome

Change in average daytime systolic blood pressure (post-exercise - pre-exercise)

Interventions

  • BEHAVIORAL Exercise

Study Locations (1)

Delaware

  • University of Delaware - Newark

Trial Details

FieldValue
Enrollment Target 30 participants
Start Date 2025-07-22
Est. Completion 2026-09
Phase NA
Freda Patterson

1 total trials

What NCT07049783 shows while recruiting

NCT07049783 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 30 participants, a relatively small participant target, below the 3,507-participant average among 470 other Hypertension trials with a reported enrollment target (99% lower).

The record links to 4 conditions, with Hypertension appearing as the primary indexed condition, and to 1 intervention - of which Exercise is the first listed.

NCT07049783 reports a single indexed study location in Delaware.

Frequently Asked Questions

What is clinical trial NCT07049783 about?

NCT07049783 is a clinical study titled "Examining the Circadian Timing Effects of the Hypotensive Response to Exercise". The goal of this study is to learn how exercise timing affects blood pressure in adults with elevated or high blood pressure. Exercise can influence the body's natural 24-hour rhythms, including blood pressure patterns. A single exercise session can lower blood pressure for up to 24 hours, but it is...

What is the current status of trial NCT07049783?

This trial is currently recruiting. It is a NA study. The enrollment target is 30 participants. The study started on 2025-07-22. Estimated completion is 2026-09.

What conditions does trial NCT07049783 study?

This clinical trial studies the following conditions: Hypertension, Circadian Rhythm, Young Adults, Post-Exercise Hypotension.

What interventions are being tested in trial NCT07049783?

The interventions under investigation include: Exercise (BEHAVIORAL).

Who is sponsoring clinical trial NCT07049783?

This trial is sponsored by Freda Patterson, which has 1 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07049783 being conducted?

This trial has 1 study location across Delaware. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Hypertension

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT07049783's enrollment target sits among peer trials

30 408th of 470 higher than 54 of 470 other Hypertension trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Hypertension trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT00977977 · 30 participants · Phase 2

    Rituximab Plus Cyclosporine in Idiopathic Membranous Nephropathy

  • NCT01459107 · 30 participants · Phase 2

    Human Upper Extremity Allotransplantation

  • NCT01666080 · 30 participants · NA

    Second or Greater Allogeneic Hematopoietic Stem Cell Transplant Using Reduced Intensity Conditioning (RIC)

  • NCT01720836 · 30 participants · Phase 1

    Study of the Immune Response of MUC1 (Mucin1) Peptide Vaccine for Non-small Cell Lung Cancer

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT07049783, the US trial registry maintained by the National Library of Medicine. NCT07049783 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.