Chrono-restricted Diet and Physical Activity as a New Preventive Strategy for Sarcopenia in Postm… (NCT07075133) | Clinical Trial Compass
Not Yet RecruitingNot Applicable
Chrono-restricted Diet and Physical Activity as a New Preventive Strategy for Sarcopenia in Postmenopausal Women With Obesity and Type 2 Diabetes
France45 participantsStarted 2026-09-15
Plain-language summary
The aim of TIMEDIAB is to demonstrate that early TRE (eTRE) combined to late (afternoon) exercise will outperform eTRE combined to morning exercise on muscle function as primary endpoint, and glucose homeostasis as secondary endpoint
Who can participate
Age range
45 Years – 70 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Post-menopausal women (amenorrhea for at least 12 months, confirmed by gonadotrophins measures)
* Age range 45-70 years
* T2DM diagnosed for more than 1 year
* Subjects with T2DM treated with lifestyle control alone or associated with metformine ± DPP4 inhibitors
* Ability to sign written informed consent before any study-specific procedure
* Subject considered as reliable and capable of adhering to protocol
* Subjects with Body Mass Index (BMI)≥ 30 kg/m²
* Baseline eating period ≥ 14 h per day (as estimated by 95% eating interval)
Exclusion Criteria:
* Subjects on T2DM injectable medication or drugs able to induce hypoglycemia (glinides, sulfonylurea)
* Subjects with HbA1c \> 8%
* Subjects with any of the following medical conditions:
* Congestive cardiac failure
* Stage 4 chronic kidney disease (i.e. eGFR \< 30 ml/min/1.73 m2)
* Liver cirrhosis or chronic liver disease
* Any medical condition that in the opinion of the investigator could jeopardize or compromise the subject's ability to participate in the study
* Subjects with previous or present history of serious eating disorder
* Subjects not able to understand the informed consent form or fasting diary instructions
* Subjects currently participating or has participated in another study of an investigational medication or an investigational medical device within the last 30 days
* Women with menopause hormone replacement therapy
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.