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The Effects of Time-Restricted Eating Model

The Effects of Time-Restricted Eating Model on Eating Behaviors, Impulsivity and Food Intake

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04960969
Enrollment
30
Registered
2021-07-14
Start date
2021-05-31
Completion date
2022-12-31
Last updated
2021-07-19

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

Conditions

Feeding Behavior, Impulsive Behavior, Time Restricted Feeding

Brief summary

There is increasing evidence of the effects of the time-restricted diet model based on the daily intake of energy within a period of 8-12 hours on body weight control and metabolic parameters. There is no study on the potential effects of this nutritional model, which is thought to be an effective strategy in struggling with metabolic syndrome, on individuals' eating behavior and impulsivity levels. This study, which aims to evaluate the effects of time- restricted diet strategy on food intake, eating attitude and behavior and impulsivity level in adults, is a mixed method, randomized controlled intervention study. Thirty adult individuals between the ages of 18-65 will be included in this study, which will be carried out between 31.05.2021-31.12.2021 in Istinye University. Participants will be divided into 2 groups: the intervention group (n = 15) will apply a time-restricted nutrition model for 4 weeks, and no intervention will be applied to the control group (n = 15). Participants' food intake before and after the intervention period will be evaluated with a 3-day food intake record, their eating attitudes will be evaluated with the Eating Attitude Test (EAT-26), their impulsivity levels will be evaluated with the Barratt Impulsiveness Scale-Short Form (BIS-11-SF) and Go / NoGo test, and their eating behaviors will be evaluated with the Three Factor Eating Questionnaire (TFEQ-R21). At the end of the research, all individuals in the intervention group will be interviewed in depth and their experiences regarding the process will be recorded. IBM SPSS 22 program will be used in the analysis of all quantitative data, and the MAXQDA-12 program will be used in the analysis of qualitative data. The data obtained from this research will clear up the applicability of the time- restricted diet model and its effects on eating behaviors of adults.

Interventions

OTHERTime-restricted feeding for 4 weeks

Participants in this group will follow a time-restricted diet for 28 days. Consumption of only non-energy drinks will be allowed for 16 hours. During the 8-hour eating period, there will be no restriction on the content of the diets.

Sponsors

Elif Emiroğlu
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
Yes

Inclusion criteria

* Being between the ages of 18-65, * Body mass index (BMI) ≥ 18.5 kg/m2, * Routine eating window ≥10 hours (including all energy-containing meals and drinks), * To agree to participate in the research voluntarily.

Exclusion criteria

* Age \<18 or \>65, * BMI \<18.5 kg/m2, * To have applied nutritional therapy for weight loss or medical treatment in the last 6 months, * Being in pregnancy or lactation period, * Working the night shift or the partner working the night shift (if it affects the participant's sleep and nutritional status), * Having a known neurological or psychological disorder, * Declaring that have a history of eating disorder in the last 3 months, * Weight change of ≥ 5 kg in the last 3 months, * Having an uncontrolled medical problem (cardiovascular, pulmonary, rheumatological, hematological, oncological, gastrointestinal, psychiatric, endocrinological, etc.) * Receiving medical treatment that may have a significant impact on glucose metabolism, appetite or energy balance, * Being on antidepressant treatment, * Having a history of bariatric surgery, * Having celiac, crohn's or ulcerative colitis.

Design outcomes

Primary

MeasureTime frameDescription
Changes in food intake of participantsBaseline and Week 4The food intake of the participants will be determined by the 3-day food consumption record at the beginning and at the 4th week.
Changes in impulsivity level of participantsBaseline and Week 4The impulsivity of the participants will be determined by the Go/NoGo Task and Short form of Barratt Impulsiveness Scale (BIS-11-SF) at the beginning and at the 4th week.
Changes in eating attitude of participantsBaseline and Week 4The eating attitude of the participants will be determined by the Eating Attitude Test (EAT-26) at the beginning and at the 4th week.
Changes in eating behaviors of participantsBaseline and Week 4The eating behaviors of the participants will be determined by the Three Factor Eating Questionnaire (TFEQ-R21) at the beginning and at the 4th week.

Countries

Turkey (Türkiye)

Contacts

Primary ContactElif Emiroğlu
elif.emiroglu@istinye.edu.tr+908502836000

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 6, 2026