Sleep Disorders Trial, Recruiting NCT07340125 Sponsor: University of South Carolina Condition: Sleep Disorders
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Sleep Disorders Trial, Recruiting

NCT07340125
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People who are male or female and between 25 and 45 years old
  • People with a body mass index (BMI) between 25.0 and 34.9, which generally falls in the overweight to moderately obese range
  • People who score 5 or higher on a standard sleep quality questionnaire called the Pittsburgh Sleep Quality Index, which indicates poor sleep quality
  • People who are generally healthy, with no diagnosed conditions affecting metabolism, heart health, or sleep
  • People who are currently not meeting standard weekly exercise guidelines — meaning less than 150 minutes of moderate exercise, less than 75 minutes of vigorous exercise, and fewer than 2 days of strength training per week
  • People who are not following a diet that restricts or eliminates certain food groups or types of food

Who may not be able to join:

  • People with a nut allergy, particularly tree nuts
  • People who have a pacemaker
  • People following a diet that restricts or eliminates certain food groups or types of food
  • People with a self-reported health condition that could affect study results, including metabolic or hormonal disorders (such as prediabetes, type 1 or type 2 diabetes, or polycystic ovary syndrome), cardiovascular disease, neuromuscular disorders, musculoskeletal disorders, or a current or recent history of cancer or cancer treatment within the past year
  • People who have had gastrointestinal surgery or a hysterectomy
  • Women who are pregnant, planning to become pregnant during the study period, pregnant within the last year, currently breastfeeding, or known to be going through perimenopause

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 12 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Katie R Hirsch, PhD, University of South Carolina

Phone: 803-777-5478

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
University of South Carolina
Registry
ClinicalTrials.gov
Start date
1 September 2025
Est. completion
1 August 2026

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

resting metabolism; exercise metabolic flexibility; post-exercise metabolism

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 12 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov