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Effects of Time of Sleep Restriction in Obesity

Effect os Sleep Restriction on Control of Food Intake and Metabolism of Obese Subjects

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01259895
Enrollment
20
Registered
2010-12-14
Start date
2009-02-28
Completion date
2012-06-30
Last updated
2014-08-18

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

Conditions

Appetite Regulation, Eating, Obesity, Sleep Restriction

Brief summary

The purpose of this study is to determine the effect of different time of sleep restriction on control of food intake and metabolism of obese and normal subjects.

Detailed description

The reduction of sleep time has now become a common habit, driven by the demands and opportunities of modern society. Some studies have suggested that sleep restriction would be an important factor in predisposing to obesity. However studies of sleep restriction in obese individuals have not yet been conducted. Still, the time of sleep restriction varies greatly between studies, making it difficult to compare results. The investigators aim to recruit 20 young adults, 10 obese and 10 normal weight individuals. The study will be conducted as a randomized, crossover study with three conditions. Each participant will be subjected to reduction of the beginning of sleep (from 3-7h), reduction of the end of sleep (from 23-3h), and normal sleep (from 23-7h), in random order, for three consecutive nights. In each condition, subjects will stay for 4 days in the laboratory. Three control meals will be offered. Visual analogue scales will be applied before and after each meal to assess hunger and appetite for different food categories. Blood samples will be collected hourly during 24 hours.

Interventions

None listed

Sponsors

Associacao Fundo de Incentivo a Psicofarmcologia
CollaboratorOTHER
Centro de Estudos em Sonolência e Acidentes
CollaboratorOTHER
Federal University of São Paulo
Lead SponsorOTHER

Study design

Observational model
CASE_CROSSOVER
Time perspective
CROSS_SECTIONAL

Eligibility

Sex/Gender
MALE
Age
20 Years to 35 Years
Healthy volunteers
Yes

Inclusion criteria

* obese (BMI\>30) and normal weight (BMI between 19 and 24,9) * regular time of sleep between 6.5 and 8 hours

Exclusion criteria

* self-reported sleep problems (Pittsburgh Sleep Quality Index score \>5); * Obstructive sleep apnea (AHI \> 5 in polysomnography) * night work; * variable sleep habits or habitual daytime naps; * regular physical exercise (\>3 hours/week); * excessive intake of alcohol (\>7 drinks/week); * excessive intake of caffeine (\>300 mg/day); * smoking; * substance abuse; * use of prescription medications or over-the-counter drugs affecting sleep or metabolism; * chronic diseases (e.g. cancer, asthma, back pain, thyroid disease, heart disease, diabetes, etc.) * history of neurological, medical or sleep disorders; * trans-meridian travelling the last month; * chronotype: extreme morning or extreme evening * unable to comply with the protocol.

Design outcomes

Primary

MeasureTime frameDescription
Appetite regulating hormones and stress hormonesMeasured every hour over the course of 24 hours on day 3Hormones are sampled from blood

Secondary

MeasureTime frameDescription
Hunger and satietyMeasured every 4 hour over the course of 12 hours on day 2 and 3Hunger and saciety are measured using visual analogue scales before and after breakfast, lunch and dinner meal
Food intakemeasured each mealThe meal will be weighted before and after the breakfast, lunch and dinner. Energy and nutrient intake are assessed from the amount of the meal consumed.

Countries

Brazil

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026