Skip to content

A randomized controlled study on the effect of time-restricted diet, half staple food combined with information-based exercise intervention on body weight and blood glucose in obese patients with abnormal blood glucose

A randomized controlled study on the effect of time-restricted diet, half staple food combined with information-based exercise intervention on body weight and blood glucose in obese patients with abnormal blood glucose

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600127375
Enrollment
Unknown
Registered
2026-06-30
Start date
2026-06-30
Completion date
Unknown
Last updated
2026-07-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Obesity

Interventions

Control group. :The control group carried out exercise intervention according to the exercise prescription provided by the "Enjoy Health" APP every week. Intervention group: all subjects were in the t
Halved staple food combined with information support exercise intervention:Group A: all subjects received half of the staple food for three meals combined with information support exercise interventio
Time-restricted eating combined with information-supported exercise intervention group.:Time-restricted diet combined with information-based support for exercise intervention group: All subjects were

Sponsors

School of Public Health, Peking University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: 1. Age 18-50 years old, both sexes; 2.BMI>=28kg/m^2; 3. Willing to cooperate with the study and sign the informed consent; 4. Permanent residents nearby; 5. Time-unlimited eating or other types of fasting habits, such as alternate-day fasting, simulated fasting diet; 6. Patients with abnormal glucose metabolism or diabetes (fasting blood glucose > 5.6mmol/L, glycosylated hemoglobin > 5.7%)

Exclusion criteria

Exclusion criteria: 1. Secondary obesity (e.g., hypothyroidism, Cushing syndrome); Use of weight-loss medications within 90 days before screening; 2. Or a weight change of more than 5 kg within 90 days before screening; 3. Pregnant, breastfeeding or planning to become pregnant; 4. Severe heart, liver and kidney dysfunction; 5. Severe mental illness or cognitive impairment, unable to cooperate with the study; 6. Presence of contraindications to exercise (e.g., severe osteoarthritis); 7. Unable or unwilling to follow the prescribed diet and exercise regimen; 8. Long-term use of medications that may significantly affect body weight; 9. Patients with active cancer in any organ system; 10. The researcher believes that the subject has any other factors that may affect the efficacy or safety assessment of this study and is not suitable to participate in this study.

Design outcomes

Primary

MeasureTime frame
Body weight;Blood glucose;

Secondary

MeasureTime frame
Body composition;Adipokine;Blood pressure;Heart rate;Fasting blood lipids;Appetite-related hormones;Sugar in urine;Urinary ketone bodies;Fecal omics;Dynamic changes of blood glucose;Fasting glucose;Fasting insulin;A 3-day 24-hour dietary review;Sleep Quality Questionnaire;The CNAQ Appetite questionnaire;Psychological questionnaire;Glycosylated hemoglobin;

Countries

China

Contacts

Public ContactXu Yaxi, Jiang Lanping

School of Public Health, Peking University

928271150@qq.com+86 181 3201 0073

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 23, 2026