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The effects of doogh on Reaction Time and alertness in comparison to water in health young adults

The effects of doogh on Reaction Time and alertness in comparision to water in healthy young adults

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017011531863N2
Enrollment
17
Registered
2017-05-11
Start date
2017-02-03
Completion date
Unknown
Last updated
2018-02-22

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

Conditions

cognitive performance and alertness-sleepiness.

Interventions

Intervention 1: Intervention: Main intervention is two hundred fifty milliliter of Doogh ( low fat and without gas), prepared in Dooka Dairy Industerial Company according to Islamic Republic of Ira
Placebo
Intervention: Main intervention is two hundred fifty milliliter of Doogh ( low fat and without gas), prepared in Dooka Dairy Industerial Company according to Islamic Republic of Iran standard for t
Control: Main intervention is two hundred fifty milliliter of natural mineral water" Seenbe" a product of Jahansoo Mineral Water Company. It will be given to each subject in two times, one in the mo

Sponsors

Morvaride Mehr Rehabilitation Center
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 40 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: Healthy human voluntaries 20-40 years; Minimum education in diploma level; General Health Questionnaire-28(GHQ-28) less than 20; Body Mass Index between 18-25; Regular sleep schedule defined by 7-8 hour sleep per night and morning wakening between 7-8 am that will be confirmed by Sleep Log; Epworth Sleepiness Scale less than 9 Exclusion criteria: Digestive problem for Doogh; Using psychiatric drugs in 3 recent months and other drugs in recent 2 weeks; History of substance and drug abuse; psychiatric and neurological disorders in past medical history; any problem in history or physical examination that interferes with using computer (e.g. orthopedic, neuromuscular, ophthalmic problems); Any disease or disorders that interfere with sleep and cognition; pregnancy; delivery within recent 18 month; Breast feeding; no stable daily shift work

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Reaction time. Timepoint: before and 120 minute after intervention. Method of measurement: TOVA software.

Secondary

MeasureTime frame
Sleepiness-alertness. Timepoint: before and 120 minutes after intervention. Method of measurement: visual analog scale.;Standard deviations of reaction time. Timepoint: before and 120 minutes after intervention. Method of measurement: TOVA software.;Comission error. Timepoint: before and 120 minutes after intervention. Method of measurement: TOVA software.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactJavad Setareh

Mazanderan University of Medical Sciences

jsetareh@mazums.ac.ir+98 11 3328 5109

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026