Time-Restricted Eating to Improve Body Composition and Symptoms in Menopause and HOrmone-sensitive Breast Cancers (TREMHO) - An Open-label Randomized Controlled Trial

Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

This study is aimed at women currently going through menopause, either as part of the natural process (physiological menopause), or following hormonal treatment for breast cancer. There are several ways of slowing the weight gain frequently encountered in this situation, reducing the intensity of menopause-related symptoms and improving quality of life in this context. In this trial, the investigators examine the efficacy and possible adverse effects of intermittent fasting compared with a control intervention. Participation lasts 14 weeks, with an optional 12-month follow-up. Study participants are randomly assigned to either the intervention group or the control group. In the intervention group, study participants fast for 16 hours per day and eat over a period of 8 hours (intermittent fasting often called time-restricted eating \[TRE\] 16h/8h). In the control group, the usual eating pattern is continued for 12 weeks. The main objective of the study is to evaluate the efficacy of TRE in terms of weight and fat loss, improvement in metabolic profile, menopausal symptoms and bone health. In addition, the study team closely monitors any adverse effects.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 45
Maximum Age: 60
Healthy Volunteers: f
View:

• Women with physiological menopause confirmed (group A) or induced menopause in the context of adjuvant therapy for hormone-sensitive non-metastatic breast cancers (group B)

• Age 40-65 years

• Body mass index 25-40 kg/m2

• Stable weight (± 2 kg) over the previous month

• Eating window ≥ 12 hours (self-reported and measured during the run-in phase)

• Able to give informed consent and follow the study procedures for the entire duration

• Confident use of a smartphone and able to take regular pictures of food/drinks

Locations
Other Locations
Switzerland
Geneva University Hospitals
RECRUITING
Geneva
Contact Information
Primary
Tinh-Hai Collet, MD
tinh-hai.collet@hug.ch
+41-22-372 91 92
Backup
Céline Joris, BSc
celine.joris@hug.ch
Time Frame
Start Date: 2025-04-30
Estimated Completion Date: 2027-03-01
Participants
Target number of participants: 84
Treatments
Experimental: Time-Restricted Eating
Active_comparator: Active Control
Related Therapeutic Areas
Sponsors
Leads: University Hospital, Geneva

This content was sourced from clinicaltrials.gov