Oxford, MSNCT06695988Now EnrollingIRB Ready

Time Restricted Eating Clinical Trial in Oxford, MS

Access cutting-edge time restricted eating treatment through this clinical trial at a research site in Oxford. Study-provided care at no cost to qualified participants.

Sponsored by University of Mississippi, Oxford

Quick Self-Assessment

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Expert Care in Oxford

Access time restricted eating specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related time restricted eating treatment provided free

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Check if you qualify for this time restricted eating clinical trial in Oxford, MS

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Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to Oxford

    Convenient for MS residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Oxford site if eligible
  4. 4Begin participation

About This Time Restricted Eating Study in Oxford

A randomized controlled trial to determine adherence, acceptability and safety of time restricted eating (TRE) in healthy, sedentary, free-living adults with obesity between the ages of 19-65 years when following 16:8 TRE for 8 weeks. This 9-week study includes a baseline week and 8 weeks of the intervention period. Participants are randomly assigned to the TRE or the non-fasting control group. The TRE group will consume calorie containing food and drink only over an 8 hour period and rest of the 16 hour would be fasting. Adherence to TRE and calorie intake are the primary outcomes. Motivators, facilitators and barriers to TRE, hunger and cravings levels, weight bias internalization, body composition (weight, body fat%, fat mass and muscle mass) , Healthy Eating Index (HEI) to assess diet quality, skin carotenoid levels, disordered eating risk, sleep quality, and perceptions of health and well-being are secondary outcomes.

Sponsor: University of Mississippi, Oxford

Who Can Participate

Inclusion Criteria

Age 19 to 65 years
Owns a smartphone
Apparently healthy
BMI ( more than or equal to 25 kg/m2 ) and high body fat percent (BF%) (≥25% and ≥35% for males and females, respectively)
Sedentary lifestyle (less than 150 minutes of self-reported moderate to vigorous activity per week)
Self-reported eating interval of ≥12 h per day

Exclusion Criteria

Diagnosed diabetes mellitus (type I or II), coronary heart disease, heart failure, hypertension, hyperlipidemia, stroke, chronic lung diseases, liver or kidney disease, adrenal diseases, musculoskeletal disorders, uncontrolled thyroid disease (dose changes within the past 3 months), Crohn's disease, Ulcerative Colitis, arthritis, undergoing active cancer treatment except for non-melanoma cancer, uncontrolled psychiatric disorder (a history of hospitalization for psychiatric illness).
Currently taking any medication that is meant for, or has a known effect on, appetite
On anabolic steroid or hormone replacement therapy
Participation in an exercise/nutrition/ weight-loss program within the last 6 months
Any history of surgical intervention for weight management
Having a ≥5% body weight change during the last 3 months
Pregnant or less than 6 months post-partum, breastfeeding, polycystic ovarian syndrome or irregular menstruation
missing limbs, have a pacemaker or metal implants,
eating disorders or EAT-26 score \>20
Alcohol or drug addiction
Current smoker
Works night shifts
Unable to commit to a 9-week study
Not willing to follow study protocol and any other contraindications.
Currently following any of the following restrictive diets - Keto/low carbohydrate/ Vegan/ Vegetarian/ Intermittent fasting/ Paleo/ Calorie restriction/ Any other restrictive diet
Participating in another 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 Oxford?

Yes, this clinical trial (NCT06695988) has an active research site in Oxford, MS 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.

Time Restricted Eating Treatment Options in Oxford, MS

If you're searching for time restricted eating treatment options in Oxford, MS, this clinical trial (NCT06695988) 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 Oxford research site is actively enrolling participants for this clinical trial. You'll receive care from experienced time restricted eating 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 time restricted eating clinical trials near you to find additional studies recruiting in your area.

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