H - Test Usage in Identification of Sexual Orientation Among People.

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: Sexual Behavior; Sexual Orientation Conflict Disorder; Sexual Arousal Disorder; Sexual Orientation; Sexual; Orientation, Relationship Disorder
• Intervention / Treatment: Diagnostic test: H - Test

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

Study Locations

• Iraq
  • Thi Qar
    • Nasiriyah, Thi Qar, Iraq, 64001
      • No name

Participation Criteria

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

How is the study designed?

Design Details

• Primary Purpose: Diagnostic
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: Double

Number of Arms

2

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.	Diagnostic test: H - Test; 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: Sexual desire test; Sexual health test
Experimental: Mustafa Ahmed Ramadhan; Is is an assessment of the vital signs among the participants and the change with the showing of videos.	Diagnostic test: H - Test; 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: Sexual desire test; Sexual health test

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	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.	1 week

Collaborators and Investigators

• Sponsor: University of Baghdad
• Investigators: Study Chair: Talib Manea, MD, University of Thi Qar

Study record dates

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: Mental Disorders; Pathologic Processes; Disease; Sexual Dysfunctions, Psychological
• 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