NCT05732935Completed
Fasting ENHANCE Pilot Study
Fasting to Provide Energy Needed to Help Adults in Need of Cognitive Enhancement (FASTING ENHANCE)
Source: ClinicalTrials.gov · Last updated 30 Jun 2026
Brief summary (registry, in English)
Grounded in the principles of geroscience, the proposed Fasting ENHANCE study will test whether a time restricted eating (TRE) regimen can improve cognitive function and other aspects of successful aging in a safe and sustainable manner in at risk overweight older adults. Specifically, this study will evaluate whether TRE can improve cognitive and physical function, as well as self-reported sleep, mood, and quality of life, in overweight, older adults (age \> 65 years) who are at high risk of cognitive decline due to self-reported cognitive difficulties. Eligible participants will be assigned to either a TRE intervention, in which they will be instructed to fast for a target of 16 hours per day, or a successful aging (SA) comparison group for a 24-week period.
- Status (registry)
- Completed
- Study type
- Interventional
- Enrollment
- 45 (actual)
- First submitted
- 11 Jan 2023
- Start date
- 13 Mar 2023
- Primary completion date
- 1 May 2026
- Lead sponsor
- University of Florida
- Diseases
- Obesity, Alzheimer disease
- NCT number
- NCT05732935
What you commit to
- Study type: Interventional
- Participants enrolled: 45
- From 13 Mar 2023 to the primary completion date, 1 May 2026
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Current use of anabolic medications (i.e., growth hormones or testosterone), antidepressant medications, antipsychotic agents, monoamine oxidase inhibitors, anticholinesterase inhibitors (i.e., Aricept), anticoagulant therapies (aspirin use is permitted), or antibiotics;
- Rheumatoid arthritis, Parkinson's disease or currently on dialysis
- Taking medications that preclude fasting for 16 hours (e.g. must be taken with food at least 12 hours apart)
- Participating in another clinical trial or has received an investigational product within 30 days prior to screening/enrollment
Other illness
- Failure to provide informed consent;
- Recent History or clinical manifestation of cardiovascular disease, diabetes, cholelithiasis, liver or renal disease, cancer, or progressive, degenerative neurologic disease (e.g., Parkinson's Disease, multiple sclerosis, ALS)
- Significant cognitive impairment, defined as a scores below the cutoff for dementia on TICS-M
- Severe rheumatologic or orthopedic diseases (e.g., awaiting joint replacement, active inflammatory disease);
- Terminal illness with life expectancy less than 12 months, as determined by a physician;
- Other significant co-morbid disease (e.g. renal failure on hemodialysis) or severe psychiatric disorder (e.g. bipolar, schizophrenia);
- History of drug or alcohol abuse (i.e., more than 5 drinks/day for males or more than 4 drinks/day for females);
- History of pulmonary disease, pneumonitis or interstitial lung disease;
- Resting heart rate of \>120 beats per minute, systolic blood pressure \> 180 mmHg or diastolic blood pressure of \> 100 mmHg
- Unstable angina, heart attack or stroke in the past 3 months
- Continuous use of supplemental oxygen to manage a chronic pulmonary condition or heart failure
- Insulin dependent diabetes mellitus
- Any condition that in the opinion of the investigator would impair ability to participate in the trial.
Lab values
- Abnormal laboratory markers (e.g., renal or liver abnormalities, elevated potassium levels, or hemoglobin and hematocrit below the lower limit of normal) as determined by study physician.
- Creatinine clearance \< 30 ml/minute by estimated Glomerular Filtration Rate (eGFR);
Other
- Excessive alcohol use (\>14 drinks per week);
- Planning to permanently leave the area in the next year;
- Current smoker or less than 3 years quit;
- Fasting \>12 hours per day
- Actively trying to lose weight by participating in formal weight loss program or significantly restricting calorie intake or weight loss \> 5 lbs in the past month
Who the study is looking for
- Age ≥ 65 years;
- Body Mass Index (BMI \> 25 kg/m2)
- Normal age-, gender-, and education-adjusted performance on TICS-M (Telephone Interview for Cognitive Status)
- Responds yes to questions 1 (memory worse), 2 (word finding difficulties) or 3 (planning/organization difficulties) on the Subjective Cognitive Decline Questionnaire
- Reports onset of cognitive difficulties in past five years
- Reports they believe they are worse than others their age OR they have talked to a clinician about it.
- Provides informed consent and willing to be randomized to either intervention group.
Age in the registry: 65 years to - · Sex: All · Accepts healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Clinical and Translational Research Building - Institute on Aging Suite Coordinator of this site? Confirm its status | Gainesville | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.