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The Efficacy of Proper Breakfast Times on Cognitive Function

U

University of Muhammadiyah Aceh

Status

Not yet enrolling

Conditions

Cognitive Change
Eating, Time Restricted
Nutrition, Healthy
Blood Pressure

Treatments

Other: breakfast 7.31 am
Other: breakfast 6.30 am

Study type

Interventional

Funder types

Other

Identifiers

NCT06541392
LP4MRiset

Details and patient eligibility

About

The goal of this cluster randomized controlled trial is to learn if a proper breakfast time may increase cognitive function. It will also learn about the effectiveness of proper breakfast time on health outcomes. The main questions it aims to answer are:

Does a proper breakfast time increase cognitive function and health outcomes?

Participants will:

  • wake up in the morning at 6 o'clock
  • Having breakfast at 6.30 - 7.30 am or 7.31-8.31 am, or having breakfast time according to their wishes.
  • Having lunch started at 12.00 pm.

Full description

This experimental study uses a Cluster Randomized Controlled Trial non-blinding parallel method design. The objective of this study is to assess the effectiveness of proper breakfast time on cognitive function including the focus on learning and mood among university students. Additionally, the study determines health outcomes such as heart rate, systolic blood pressure, diastolic blood pressure, and macro and micronutrient intake. There are a total of 60 participants from three different faculties. All faculties will be randomly selected and assigned to intervention group 1, intervention group 2, and the control group. Each group consists of 20 participants from each faculty in the university. Intervention Group 1 will have breakfast from 6:30 to 7:30 am, and Intervention Group 2 from 7:31 to 8:31 am. Meanwhile, the control group will continue their preferred breakfast routine. The intervention groups are required to wake up at 6:00 am and have lunch at 12:00 pm.

Enrollment

60 estimated patients

Sex

All

Ages

18 to 24 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Active student in the year 2024
  • Not in medication
  • Do not have gastritis or any diseases that require to have breakfast earlier in the morning
  • Willing to sign an informed consent
  • Have health insurance

Exclusion criteria

  • Abstain in the education session
  • Having emotional and mental health problems
  • Students in the final class who are undergoing the thesis writing

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

60 participants in 3 patient groups

Breakfast1
Experimental group
Description:
This group will have breakfast time at 6.30 to 7.30 am
Treatment:
Other: breakfast 6.30 am
Breakfast2
Experimental group
Description:
This group will have breakfast time from 7.31 am to 8.31 am
Treatment:
Other: breakfast 7.31 am
Control
No Intervention group
Description:
This group will have breakfast time according to their wishes.

Trial contacts and locations

0

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Central trial contact

Maidar Abdul Manan, Ph.D; Dharina Baharuddin, MPH

Data sourced from clinicaltrials.gov

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