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Investigating the effect of Descurainia sophia (L.) Webb ex prantl on hydration, thirst status, and fatigue in recreational athletes

Comparison the effect of Descurainia sophia (L.) Webb ex prantl on hydration, thirst status, and fatigue in recreational athletes

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20201010048982N3
Enrollment
32
Registered
2024-11-04
Start date
2024-11-21
Completion date
Unknown
Last updated
2025-01-08

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

Conditions

Investigating the state of hydration, thirst and fatigue in non-professional athletes.

Interventions

Intervention 1: Intervention group: Non-professional cyclists drank a syrup containing 2 grams of Descurainia sophia powder and 6.25 grams of brown sugar per 100 ml at a temperature of 15 degrees Cels

Sponsors

Oroumia University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: - Non-professional cyclists 18-40 years old who volunteered to participate in the study with BMI in the normal range (24/9-18/9)

Exclusion criteria

Exclusion criteria: - Diagnosis of any systemic disease that may be aggravated by participating in the study - People with abnormal liver function or abnormal kidney function - Women who are pregnant or breastfeeding, or intending to become pregnant - People with blood pressure above 140/90 mmHg or high blood pressure with the use of a diuretic - People with a history of asthma or allergic disease - People with a history of alcohol addiction, drug addiction, or mental illness - People with chronic cardiovascular, metabolic, respiratory diseases, recent muscle and skeletal injuries, previous history of heat stroke during the last 3 years - People with a history of hay fever allergy based on self-report

Design outcomes

Primary

MeasureTime frame
Thirst evaluation questionnaire will be done at the beginning of the trial and after the end of the study period using the thirst evaluation questionnaire and visual analog scale (VAS) 10 cm self-rating, where zero means no desire to consume liquids and ten means It means extreme thirst.The volunteers' fatigue assessment questionnaire will be completed by the volunteers at the beginning of the trial (minute zero) and after the study period.The volunteers' urine samples will be taken at 0 (before the start of running), 45, 70, 95 and 120 minutes during the trial and will be collected in urine sample containers for analysis. The color and specific density of urine will be measured visually and using a digital refractometer at the mentioned time intervals. Timepoint: The test will be conducted in controlled conditions (temperature 35°C, relative humidity 30% and cooler temperature 26°C) on a treadmill for 45 minutes.Urine samples of volunteers will be taken at 0 (before the start of running), 45, 70, 95 and 120 minutes during the trial and will be collected in urine sample containers for analysis.Volunteers' blood samples will be taken at 0, 45, and 120 minutes during the trial, and blood analyzes will be performed including measurement of plasma volume and hematocrit.The heart rate of the volunteers will be measured at 0, 45, 70, 95 and 120 minutes during the trial period. Thirst evaluation questionnaire at the beginning of the experiment and after the end of the study period will be completed by the volunteers using the thirst evaluation questionnaire and the fatigue evaluation questionnaire of the volunteers at the beginning of the experiment (zero minute) and after the study. Method of measurement: Fatigue and thirst questionnaire, refractometer and blood tests to check the specific density of urine.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactSevana Dangian

Oroumia University of Medical Sciences

far.alami28@gmail.com+98 45 3333 7906

Outcome results

None listed

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