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NCT06365723 · ClinicalTrials.gov registry record · NA

Effects of Walking in Greenspace and the Built Environment in Adults With Prediabetes: A Randomized Crossover Trial

A NA study of PreDiabetes and Heart Rate Variability (HRV), sponsored by University of Minnesota.

Recruiting
Registry status
NA
Development phase
216
Enrollment target
3
Study locations

NCT06365723 is a NA study of PreDiabetes and Heart Rate Variability (HRV) that is actively recruiting participants, run by University of Minnesota. The registered enrollment target is 216 participants, below the 689-participant average among 89 other PreDiabetes trials with a reported enrollment target (69% lower). The trial reports 3 study locations across 2 states.

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The verdict

NCT06365723, a NA study of PreDiabetes and Heart Rate Variability (HRV), is actively recruiting participants, sponsored by University of Minnesota.

RECRUITING
Registry status
NA
Development phase
216 participants
Enrollment target
3
Study locations

Study Summary

The goal of this randomized crossover trial is to compare the differences in psychological and physiological effects of walking in two different outdoor environments (urban/suburban commercial environments vs. urban/suburban nature areas/preserves) in adults with prediabetes. The main questions it aims to answer are: * Do psychological measures of stress, anxiety, and affect improve more in one type of outdoor environment over the other? * Do physiological measures of stress improve more in one type of outdoor environment over the other? As this is a crossover trial, participants will serve as their own controls. Researchers will compare both the psychological and physiological effects walking in the two types of outdoor environments. Participants will: * Walk 150-minutes per week for six weeks in each of the two outdoor conditions. * Visit the clinic four times, including before and after each six-week walking period. * Collect saliva samples immediately proceeding or following the four clinic visits. * Return to their pre-study level of physical activity for a 5-week washout period between each of the two walking interventions.

Interventions

  • BEHAVIORAL Nature-based Walking
  • BEHAVIORAL Built-environment/Commercial Walking

Study Locations (3)

Illinois

  • Lake Forest Hospital - Lake Forest
  • Central DuPage Hospital - Winfield

Minnesota

  • Epidemiological Clinical Research Center - Minneapolis

Trial Details

FieldValue
Enrollment Target 216 participants
Start Date 2024-06-06
Est. Completion 2027-11-30
Phase NA

Sponsor

University of Minnesota

966 total trials

What the Registry Record Tells You About NCT06365723

The ClinicalTrials.gov registry entry for NCT06365723 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 216 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 689-participant average among 89 other PreDiabetes trials with a reported enrollment target (69% lower). The listed sponsor is University of Minnesota, which has 966 total studies on file at ClinicalTrials.gov.

The record links to 4 conditions, with PreDiabetes appearing as the primary indexed condition, and to 2 interventions - of which Nature-based Walking is the first listed.

NCT06365723 reports 3 study locations spanning 2 distinct geographic areas - top geographies include Illinois, Minnesota.

Frequently Asked Questions

What is clinical trial NCT06365723 about?

NCT06365723 is a clinical study titled "Effects of Walking in Greenspace and the Built Environment in Adults With Prediabetes: A Randomized Crossover Trial". The goal of this randomized crossover trial is to compare the differences in psychological and physiological effects of walking in two different outdoor environments (urban/suburban commercial environments vs. urban/suburban nature areas/preserves) in adults with prediabetes. The main questions it a...

What is the current status of trial NCT06365723?

This trial is currently recruiting. It is a NA study. The enrollment target is 216 participants. The study started on 2024-06-06. Estimated completion is 2027-11-30.

What conditions does trial NCT06365723 study?

This clinical trial studies the following conditions: PreDiabetes, Heart Rate Variability (HRV), Stress and Anxiety, Stress Biomarkers.

What interventions are being tested in trial NCT06365723?

The interventions under investigation include: Nature-based Walking (BEHAVIORAL), Built-environment/Commercial Walking (BEHAVIORAL).

Who is sponsoring clinical trial NCT06365723?

This trial is sponsored by University of Minnesota, which has 966 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06365723 being conducted?

This trial has 3 study locations across Illinois, Minnesota. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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