- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06388928
Effect of Menstrual Cycle on the Manual Dexterity of Female Dentists
April 24, 2024 updated by: Amira Ibrahim Hassanein Abdel-aal, Cairo University
The aim of this observational study was to investigate the effect of the menstrual cycle on the manual dexterity of female dentists.
This study was conducted to answer the following question:
- Is there any effect of the menstrual cycle on the manual dexterity of female dentists?
Study Overview
Status
Completed
Conditions
Study Type
Observational
Enrollment (Actual)
45
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Damietta, Egypt
- Horus University
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
N/A
Sampling Method
Non-Probability Sample
Study Population
Forty-five nulliparous female dentists, with at least one year of practice of the manual work, participated in this study.
They were recruited from the outpatient clinic of the Faculty of Dentistry, Horus University, and from private dental clinics.
Description
Inclusion Criteria:
- All participants were nulliparous female dentists having a regular menstrual cycle which was confirmed by using a calendar of three consecutive menstrual cycles.
- Their ages ranged from 25 to 35 years old.
- Their BMI was within the normal range (18.5 to 24.9 kg/m²).
Exclusion Criteria:
- Pregnant female dentists.
- Irregular menstrual cycle and any type of hormonal therapy that may affect normal hormonal level fluctuation.
- History of either orthopedic or neurologic diseases causing functional defects of hand strength such as fracture, carpal tunnel syndrome, or De-Quervain's syndrome.
- Upper limb or hand surgery.
- History of systemic diseases like diabetes mellitus.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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This study was assigned as a single group.
All participants, assigned as one group, were assessed as regards the manual dexterity at three different phases of the menstrual cycle (menstrual phase, ovulation phase, and mid-luteal phase).
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Manual dexterity assessment
Time Frame: Assessment of the female dentists' manual dexterity was performed from July 2023 to December 2023
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Purdue pegboard test (Lafayette, IN 47093 USA, Model 32020A) was used to measure the participants' unimanual and bimanual hand dexterity.
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Assessment of the female dentists' manual dexterity was performed from July 2023 to December 2023
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Amira I Hassanein, Cairo University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
July 9, 2023
Primary Completion (Actual)
December 26, 2023
Study Completion (Actual)
December 26, 2023
Study Registration Dates
First Submitted
January 17, 2024
First Submitted That Met QC Criteria
April 24, 2024
First Posted (Actual)
April 29, 2024
Study Record Updates
Last Update Posted (Actual)
April 29, 2024
Last Update Submitted That Met QC Criteria
April 24, 2024
Last Verified
January 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- P.T.REC/012/004596
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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