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A study on the safety and effectiveness of "a weight loss program by setting energy intake considering changes in basal metabolic rate"

A study on the safety and effectiveness of "a weight loss program by setting energy intake considering changes in basal metabolic rate" - A weight loss program by setting energy intake considering changes in basal metabolic rate

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000044385
Enrollment
20
Registered
2021-06-01
Start date
2021-06-01
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Obesity

Interventions

Providing an appropriate diet based on resting metabolic rate and physical activity (24 weeks)

Sponsors

Department of Endocrinology and Diabetes, Nagoya University Graduate School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Patients with obesity 2) Patients who are aged >=18 years and <65 years 3) Patients who have not participated in other weight loss programs in the last 8 weeks 4) Patients who provide their consent in a written form by themselves

Exclusion criteria

Exclusion criteria: The exclusion criteria are as follows: 1) Secondary obesity (symptomatic obesity) 2) Patients who had a history of highly invasive surgery, severe trauma, severe infection disease, malignant tumor, or hyperthyroidism within six months 3) Patients with severe impairment in cardiorespiratory, renal or liver function to whom exercise therapy is not applicable (includes patients estimated glomerular filtration rate < 30 mL/min/1.73 m2) 4) Patients with severe musculoskeletal impairment to whom exercise therapy is not applicable 5) Patients who are pregnant, suspected of being pregnant, within 28 days of parturition, or breastfeeding 6) Patients who are judged by their physicians to be unsuitable for participation in the study

Design outcomes

Primary

MeasureTime frame
Change in body weight

Secondary

MeasureTime frame
Changes in resting metabolic rate, body composition, and BMI Changes in HbA1c level, lipids, and blood pressure Changes in various blood and urine test items Changes in calorie intake Changes in physical activity Change in hunger scale 3% or 5% weight loss achievement rate Adverse events (safety) An exploratory study in patients with high weight loss

Countries

Japan

Contacts

Public ContactTakeshi Onoue

Nagoya University Graduate School of Medicine Department of Endocrinology and Diabetes

t-onoue@med.nagoya-u.ac.jp052-744-2142

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026