Is NCT06365723 recruiting in Winfield, IL?

Yes, NCT06365723 is currently recruiting participants at its Winfield, IL location. This prediabetes clinical trial is actively enrolling qualified participants.

How do I join the prediabetes clinical trial in Winfield?

To join this clinical trial in Winfield, complete the eligibility form on this page. A study coordinator will contact you to discuss next steps and determine if you qualify.

Is participation in this Winfield clinical trial free?

Yes, all study-related care is provided at no cost to qualified participants. Many studies also offer compensation for time and travel expenses.

PreDiabetes Clinical Trial in Winfield, IL

About This PreDiabetes Study in Winfield

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.

Sponsor: University of Minnesota

Who Can Participate

Inclusion Criteria

25-64 years old.

Classified as overweight or obese with BMI 20.0-39.9 kg/m2 per self-report and a BMI of 20.0- 41.9 kg/m2 upon actual measure.

Documentation\

of a PreD diagnosis within one year of enrollment by physician or primary care provider based on lab tests showing a fasted blood glucose of 100-125 mg/dL, a 2-hour oral glucose tolerance test of 140-199 mg/dL, or an HbA1c level of 5.7%-6.49%271; OR a study screening lab value of HbA1C within the aforementioned range.

Currently engaged in ≤100 min/week of moderate to vigorous exercise -confirmed via a 7-day activity recall.

No exercise contraindications as assessed by the Physical Activity Readiness Questionnaire (PAR-Q) -this Questionnaire involves seven "yes" or "no" questions regarding an individual's health status. Answering "yes" to any one of these questions may require a prospective participant to acquire a written doctor's note stating they can safely participate in the trial's exercise intervention. The participant would not be enrolled until this doctor's note is received.

Stable weight over the last 3 months (less than 10% change).

Not currently pregnant, planning to become pregnant, or currently breastfeeding.

Willing to maintain current dietary and exercise habits, aside from any changes to be made per the study exercise protocol.

Must own a smartphone and be willing and able to download the Garmin Connect app

Ability to speak and understand English.

Any level of income

Any race/ethnicity

Exclusion Criteria

Individuals \<25 or \>64: younger individuals may have not yet reached physiological maturity and in whom PreD prevalence is low; older individuals are more likely to have contraindications to PA and other comorbidities.

BMI \<20 or ≥42.

Individuals with an HbA1c level \<5.7% or \>6.4%.

Currently engaged in \>100 min/wk of PA.

Individuals with contraindications to exercise participation as indicated by the PAR-Q.

A self-reported physical/mental disability that would prevent them from being able to adhere to the intervention.

Past or current diagnosis of Diabetes (Type 1, 1.5 or 2) or use of diabetic medications (e.g. medications to control blood sugar)

Any history of a cardiovascular disease event (e.g. heart attack, ablation, pacemaker, stroke)

Current treatment for cancer or heart disease (lipid and hypertensive medications acceptable but will be tracked closely).

Any change within the last 3 months, or anticipated changes, of any medications that would affect study outcomes (e.g. medications for lipids, blood pressure, anxiety, depression)

The use of any medication that significantly interferes with the autonomic nervous system

Current tobacco or nicotine users, or those who have quit within the last six months

Excessive alcohol (on average\>1 drinks/day for women and \>2 drinks/day for men) or excessive recreational drug use (reported usage of once a week or more).

Unstable weight over the last three months (\>10% change).

Those with major surgery planned or recent history of bariatric surgery (within last 2 years) or a history of other medical interventions that would interfere with study outcomes

Currently within one-year postpartum, currently pregnant, or planning to become pregnant during the study period.

Currently breastfeeding.

Unwilling to comply with study randomization procedures.

Unwilling to maintain current dietary and exercise habits, aside from any changes to be made per the study exercise protocol.

Current participation in another interventional clinical trial.

Previous randomization in this study.

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Winfield?

Yes, this clinical trial (NCT06365723) has an active research site in Winfield, IL that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

PreDiabetes Treatment Options in Winfield, IL

If you're searching for prediabetes treatment options in Winfield, IL, this clinical trial (NCT06365723) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Winfield research site is actively enrolling participants for this clinical trial. You'll receive care from experienced prediabetes specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

Looking for more options? Browse all prediabetes clinical trials near you to find additional studies recruiting in your area.

PreDiabetes Clinical Trial in Winfield, IL

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