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Time-Restricted Feeding for the Prevention and Therapy of Lifestyle-dependent Disease

Time-Restricted Feeding for the Prevention and Therapy of Lifestyle-dependent Disease - TRF-Pilot

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00015057
Enrollment
90
Registered
2018-08-10
Start date
2018-09-10
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

Prevention and therapy of lifestyle-dependent disease

Interventions

Group 1: Intervention in Healthy participants: restriction of the daily intake of solid food to 8-9 hours is carried out for a period of three months. Group 2: Intervention in patients with any compon

Sponsors

Institut für Allgemeinmedizin, Universität Ulm
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 67 Years

Inclusion criteria

Inclusion criteria: Arm 1: Employees of the University/University Hospital Ulm, no known metabolic diseases, no known eating disorders. Arm 2: Patients of the GP's practice with characteristics of metabolic syndrome without eating disorders, no insulin-dependent diabetes, no hyperthyroidism

Exclusion criteria

Exclusion criteria: Contraindications for fasting

Design outcomes

Secondary

MeasureTime frame
Secondary outcome measures are longitudinal changes in anthropometric parameters (height, weight, waist circumference) and laboratory parameters (fasting glucose, IGF-1, triglycerides, cholesterol, HDL, LDL, cortisol, LDH, CRP) as well as health-related quality of life (VAS from EQ-5D), sleep duration and quality. These data are collected at the two measurement points before and after the intervention.

Primary

MeasureTime frame
Primary outcome measure is the achievement of the target period of 8-9 hours of food intake (recorded in a diary: time of first and last meal). For this purpose, the percentage of days with the achievement of the target over the entire study period is calculated for each participant.

Countries

Germany

Contacts

Public ContactDorothea Kesztyüs

Institut für Allgemeinmedizin, Universität Ulm

dorothea.kesztyues@uni-ulm.de0731/500 31102

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 17, 2026