NCT05999071

Brief Summary

C. sativum could potentially serve as a memory enhancer for university students. It is considered a preferable option to stimulant drugs due to its safety profile. Additionally, C. sativum may have positive effects on anxiety, depression, and sleep quality. However, it is important to note that the current body of research on the effects of oral C. sativum on the brain and nervous system is limited, and further studies are necessary to fully understand its potential benefits. Thus, this study aims to assess the impact of oral C. sativum on memory performance, anxiety, depression, and sleep quality in university students.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
86

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Mar 2022

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

March 1, 2022

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 1, 2022

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

July 1, 2022

Completed
1.1 years until next milestone

First Submitted

Initial submission to the registry

August 3, 2023

Completed
18 days until next milestone

First Posted

Study publicly available on registry

August 21, 2023

Completed
Last Updated

August 21, 2023

Status Verified

August 1, 2023

Enrollment Period

4 months

First QC Date

August 3, 2023

Last Update Submit

August 11, 2023

Conditions

Keywords

Coriandrum sativummemory performanceanxietydepressionsleep

Outcome Measures

Primary Outcomes (1)

  • Memory performance

    Prospective and Retrospective Memory Questionnaire was performed

    30 days

Secondary Outcomes (2)

  • Anxiety and depression

    30 days

  • Sleep quality

    30 days

Study Arms (2)

Coriandrum sativum group

EXPERIMENTAL

500 mg of C. sativum (capsules) were administered twice daily

Dietary Supplement: Coriandrum sativum seeds

control group

PLACEBO COMPARATOR

500 mg of starch (capsules) were administered twice daily

Dietary Supplement: Coriandrum sativum seeds

Interventions

Coriandrum sativum seedsDIETARY_SUPPLEMENT

Each group consisted of 50 students. In the C. sativum group, dried powdered seeds of C. sativum were administered, while in the control group, starch was provided as a placebo. Both the C. sativum and placebo capsules were identical in shape, color, and outer packaging to maintain the blinding of the participants.

Also known as: Coriandrum
Coriandrum sativum groupcontrol group

Eligibility Criteria

Age19 Years - 23 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Male or female university Student.
  • of age

You may not qualify if:

  • Medical diseases.
  • Psychiatric disorders.
  • Using any form of medication (including complementary and alternative medicines).
  • Pregnant and lactating individuals.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Faculty of Pharmaceutical Sciences

Zarqa, 13133, Jordan

Location

MeSH Terms

Conditions

Memory DisordersAnxiety DisordersDepression

Interventions

coriander oil

Condition Hierarchy (Ancestors)

Neurobehavioral ManifestationsNeurologic ManifestationsNervous System DiseasesSigns and SymptomsPathological Conditions, Signs and SymptomsMental DisordersBehavioral SymptomsBehavior

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
TRIPLE
Who Masked
PARTICIPANT, CARE PROVIDER, INVESTIGATOR
Purpose
SUPPORTIVE CARE
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Assisstant professor

Study Record Dates

First Submitted

August 3, 2023

First Posted

August 21, 2023

Study Start

March 1, 2022

Primary Completion

July 1, 2022

Study Completion

July 1, 2022

Last Updated

August 21, 2023

Record last verified: 2023-08

Data Sharing

IPD Sharing
Will not share

All participants data will be hidden

Locations