H - Test Usage in Identification of Sexual Orientation Among People.
Primary Purpose
Sexual Behavior, Sexual Orientation Conflict Disorder, Sexual Arousal Disorder
Status
Completed
Phase
Not Applicable
Locations
Iraq
Study Type
Interventional
Intervention
H - Test
Sponsored by
About this trial
This is an interventional diagnostic trial for Sexual Behavior
Eligibility Criteria
Inclusion Criteria:
- All the people can be included
Exclusion Criteria:
- Have a psychological disorder
- Have a sexual disorder
Sites / Locations
- No name
Arms of the Study
Arm 1
Arm 2
Arm Type
Other
Experimental
Arm Label
Hashim Talib Hashim
Mustafa Ahmed Ramadhan
Arm Description
It is a video with +18 different contents to know the effect of much video than the others.
Is is an assessment of the vital signs among the participants and the change with the showing of videos.
Outcomes
Primary Outcome Measures
An observatory stimulation test of sexual orientation (Straight, gay, lesbian, bisexual) by using videos stimulation
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.
Secondary Outcome Measures
Full Information
NCT ID
NCT04673708
First Posted
November 28, 2020
Last Updated
October 31, 2022
Sponsor
University of Baghdad
1. Study Identification
Unique Protocol Identification Number
NCT04673708
Brief Title
H - Test Usage in Identification of Sexual Orientation Among People.
Official Title
Using H - Test to Identify the Sexual Orientation and Applying the Test in Medical and Forensic Fields
Study Type
Interventional
2. Study Status
Record Verification Date
October 2022
Overall Recruitment Status
Completed
Study Start Date
December 11, 2020 (Actual)
Primary Completion Date
December 25, 2020 (Actual)
Study Completion Date
December 26, 2020 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Baghdad
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Using of H - test in identifying the sexual behavior of the human.
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.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sexual Behavior, Sexual Orientation Conflict Disorder, Sexual Arousal Disorder, Sexual Orientation, Sexual; Orientation, Relationship Disorder
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare Provider
Allocation
Randomized
Enrollment
55 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Hashim Talib Hashim
Arm Type
Other
Arm Description
It is a video with +18 different contents to know the effect of much video than the others.
Arm Title
Mustafa Ahmed Ramadhan
Arm Type
Experimental
Arm Description
Is is an assessment of the vital signs among the participants and the change with the showing of videos.
Intervention Type
Diagnostic Test
Intervention Name(s)
H - Test
Other Intervention Name(s)
Sexual desire test, Sexual health test
Intervention Description
Showing different videos for a sexual stimulus and monitor the vitals of each participants to measure any changes can occur with each video.
Primary Outcome Measure Information:
Title
An observatory stimulation test of sexual orientation (Straight, gay, lesbian, bisexual) by using videos stimulation
Description
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.
Time Frame
1 week
10. Eligibility
Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
All the people can be included
Exclusion Criteria:
Have a psychological disorder
Have a sexual disorder
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Talib Manea, MD
Organizational Affiliation
University of Thi Qar
Official's Role
Study Chair
Facility Information:
Facility Name
No name
City
Nasiriyah
State/Province
Thi Qar
ZIP/Postal Code
64001
Country
Iraq
12. IPD Sharing Statement
Plan to Share IPD
Yes
IPD Sharing 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
Learn more about this trial
H - Test Usage in Identification of Sexual Orientation Among People.
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