- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04673708
H - Test Usage in Identification of Sexual Orientation Among People.
October 31, 2022 updated by: Hashim Talib Hashim, University of Baghdad
Using H - Test to Identify the Sexual Orientation and Applying the Test in Medical and Forensic Fields
Using of H - test in identifying the sexual behavior of the human.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
The test using videos and in the same time watching the vital signs of the participant to identify any changes in them align with the vides.
These videos contain +18 contents that can excite them and make them sexually active. So we can determine with type of vides that more excited to the human and select his or her sexual behavior type.
Study Type
Interventional
Enrollment (Actual)
55
Phase
- Not Applicable
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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Thi Qar
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Nasiriyah, Thi Qar, Iraq, 64001
- No name
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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
20 years to 60 years (Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Description
Inclusion Criteria:
- All the people can be included
Exclusion Criteria:
- Have a psychological disorder
- Have a sexual disorder
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
- Primary Purpose: Diagnostic
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Other: Hashim Talib Hashim
It is a video with +18 different contents to know the effect of much video than the others.
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Showing different videos for a sexual stimulus and monitor the vitals of each participants to measure any changes can occur with each video.
Other Names:
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Experimental: Mustafa Ahmed Ramadhan
Is is an assessment of the vital signs among the participants and the change with the showing of videos.
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Showing different videos for a sexual stimulus and monitor the vitals of each participants to measure any changes can occur with each video.
Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
An observatory stimulation test of sexual orientation (Straight, gay, lesbian, bisexual) by using videos stimulation
Time Frame: 1 week
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Using the test to arouse the sexual state among the participants by using sexual videos either for gays or straights, that can stimulate them sexually while monitoring their vitals to see the changes that can occur with each videos and the most effective video will be considered as a sufficient stimulus.
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1 week
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Chair: Talib Manea, MD, University of Thi Qar
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)
December 11, 2020
Primary Completion (Actual)
December 25, 2020
Study Completion (Actual)
December 26, 2020
Study Registration Dates
First Submitted
November 28, 2020
First Submitted That Met QC Criteria
December 11, 2020
First Posted (Actual)
December 17, 2020
Study Record Updates
Last Update Posted (Actual)
November 1, 2022
Last Update Submitted That Met QC Criteria
October 31, 2022
Last Verified
October 1, 2022
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- H98
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Yes
IPD Plan Description
No personal data will be shared with others except the data used to state the study measures.
IPD Sharing Time Frame
They will be available in three months and for six months.
IPD Sharing Access Criteria
They will shared on drive
IPD Sharing Supporting Information Type
- Study Protocol
- Statistical Analysis Plan (SAP)
- Informed Consent Form (ICF)
- Clinical Study Report (CSR)
- Analytic Code
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.