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

NCT03001427 · ClinicalTrials.gov registry record · NA

Neurocognition, Lifestyle Modification, and Treatment Resistant Hypertension

A NA study, sponsored by Duke University.

Completed
Registry status
NA
Development phase
140
Enrollment target

NCT03001427: Completed NA study, sponsored by Duke University.

NCT03001427 is a NA study that has completed, run by Duke University. The registered enrollment target is 140 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (90% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT03001427, a NA study, has completed, sponsored by Duke University.

COMPLETED
Registry status
NA
Development phase
140 participants
Enrollment target

Study Summary

This application proposes to extend an ongoing NHLBI clinical trial (NCT02342808) examining the efficacy of a lifestyle intervention combining the Dietary Approaches to Stop Hypertension (DASH) diet with caloric restriction and aerobic exercise to lower and control BP in individuals with RH. In the parent trial, participants with RH will be randomized to either: (1) a 4-month adjunctive lifestyle intervention designed to lower BP through exercise and diet (C-LIFE), or; (2) a standardized education and physician advice (SEPA) control condition. The current protocol will collect additional assessments of neurocognition (executive function, processing speed, and memory), endothelial function (brachial artery flow-mediated dilation), and cerebrovascular reserve (a measure of prefrontal cortex tissue oxygenation) in 120 participants at baseline, following completion of the 4-month intervention, and again after one year, in order to examine neurocognitive improvements and their potential mediators.

Primary Outcome

Trail Making Test Part B, Stroop Color-Word Section, Animal Naming, COWA, CVLT-II Discrimination Index

Interventions

  • BEHAVIORAL Structured center-based lifestyle intervention
  • BEHAVIORAL Standard education and physician advice

Trial Details

FieldValue
Enrollment Target 140 participants
Start Date 2016-01
Est. Completion 2020-12-14
Phase NA
Duke University

1,725 total trials

What the finished NCT03001427 record still lists

NCT03001427 is an interventional study that assigns participants to a tested intervention. The registered 140 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (90% lower).

The record links to 0 conditions, and to 2 interventions - of which Structured center-based lifestyle intervention is the first listed.

NCT03001427 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT03001427 about?

NCT03001427 is a clinical study titled "Neurocognition, Lifestyle Modification, and Treatment Resistant Hypertension". This application proposes to extend an ongoing NHLBI clinical trial (NCT02342808) examining the efficacy of a lifestyle intervention combining the Dietary Approaches to Stop Hypertension (DASH) diet with caloric restriction and aerobic exercise to lower and control BP in individuals with RH. In the ...

What is the current status of trial NCT03001427?

This trial is currently completed. It is a NA study. The enrollment target is 140 participants. The study started on 2016-01. Estimated completion is 2020-12-14.

What interventions are being tested in trial NCT03001427?

The interventions under investigation include: Structured center-based lifestyle intervention (BEHAVIORAL), Standard education and physician advice (BEHAVIORAL).

Who is sponsoring clinical trial NCT03001427?

This trial is sponsored by Duke University, which has 1,725 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT03001427's enrollment target sits among peer trials

140 713th of 2000 higher than 1,281 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA 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

  • NCT01419561 · 140 participants · Phase 2

    Natural History Study of the KSHV Inflammatory Cytokine Syndrome (KICS)

  • NCT01624805 · 140 participants · Phase 2

    Methylprednisolone, Horse Anti-Thymocyte Globulin, Cyclosporine, Filgrastim, and/or Pegfilgrastim or Pegfilgrastim Biosimilar in Treating Patients With Aplastic Anemia or Low or Intermediate-Risk Myelodysplastic Syndrome

  • NCT02369770 · 140 participants · NA

    Sensory-Motor Rehabilitation Post Stroke

  • NCT02455193 · 140 participants · NA

    Neuronal Effects of Exercise in Schizophrenia

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT03001427, the US trial registry maintained by the National Library of Medicine. NCT03001427 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.