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TRE: Microbiome, Metabolic Health and Bone (TREMBO)

Rutgers The State University of New Jersey logo

Rutgers The State University of New Jersey

Status

Active, not recruiting

Conditions

Weight Loss
Time Restricted Feeding
Bone Loss

Treatments

Behavioral: Calorie Restriction
Behavioral: Time Restricted Eating (TRE)

Study type

Interventional

Funder types

Other

Identifiers

NCT05548517
Pro2021002434

Details and patient eligibility

About

In the Time-Restricted Eating: Microbiome and Bone (TREMBO) study, the primary goal is to determine the effect of time-restricted eating with caloric restriction compared to caloric restriction alone on body weight, the gut microbiota, and bone health in older women who are overweight or obese.

Full description

Time-restricted eating (TRE) has gained increased attention due to the possibility to induce weight loss and improve cardiometabolic health as a result of the purported alignment of circadian rhythm. However, since TRE is often reported to cause a spontaneous reduction of calories, it is not well understood if these health benefits are due to weight loss, circadian rhythm alignment, or a combination of the two. Furthermore, while weight loss can improve cardiometabolic health, it can also induce bone loss, which is problematic in older women who are at a higher risk of fracture. Interestingly, both bone turnover and the gut microbiota are responsive to diurnal variations, such as meal timing, and alterations in the gut microbiota have been associated with differences in bone health. In rodent models, caloric restriction can alter the gut microbiota composition with further alterations shown due to time-restricted eating. This suggests that time-restricted eating could affect bone health, which may be partially mediated by changes in the gut microbiota. Also, lifestyle patterns affects both the microbiota and bone. This randomized controlled trial will use behavior modification to examine TRE plus caloric restriction (CR) to achieve an evening energy deficit compared to CR alone on body weight, the gut microbiota, and bone health in older women who are overweight or obese.

Enrollment

48 estimated patients

Sex

Female

Ages

50 to 79 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Postmenopausal women (>2 years since last menses)
  • Body mass index (25-45 kg/m2)
  • Agree to be randomly assigned to consume food for ≤ 9 hours/day or ≥12 hours/day
  • Must attend on-site visits (about 10) in New Brunswick, NJ, USA (transportation/reimbursement for travel not included)

Exclusion criteria

  • Participants with >5% weight loss in the past 6 months or extreme dietary/physical activity habits
  • An inability to follow the experimental intervention or to perform the required specimen collections
  • Antibiotic use in the past 2 months
  • Current diagnosis, or history of cancer in past 3 years
  • History of surgical procedure for weight loss in the past 3 years
  • Current diagnosis or history of bone diseases, type I or II diabetes, gastrointestinal disease, hyperparathyroidism, untreated thyroid disease, significant immune, hepatic, cardiac, or renal disease
  • Uncontrolled hypertension or hyperlipidemia in abnormal ranges
  • Regular use of medications that affect bone metabolism, including bisphosphonates or hormone replacement.
  • A colonoscopy within the past 2 months
  • Alcohol or illicit drug abuse
  • Current smoker or having quit smoking in the past 3 months
  • Shift work
  • Participation in another clinical research trial which may interfere with the results of this study.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

48 participants in 2 patient groups

Time restricted eating and calorie restriction
Experimental group
Description:
Subjects will be asked to adhere to a calorie-restricted diet and will be counseled by a dietitian for diet and lifestyle behavior education. In addition, they will be asked to only consume calories during a 9-hour window (15:9).
Treatment:
Behavioral: Time Restricted Eating (TRE)
Behavioral: Calorie Restriction
Calorie restriction alone
Active Comparator group
Description:
Subjects will be asked to adhere to a calorie-restricted diet and will be counseled by a dietitian for diet and lifestyle behavior education. They will be advised to continue to consume foods throughout the day and into the evening.
Treatment:
Behavioral: Calorie Restriction

Trial contacts and locations

1

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Central trial contact

Brandon McGuire; Prinicipal Investigator

Data sourced from clinicaltrials.gov

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