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

NCT04673708 | Completed DMC

• 1 other identifier: H98
• Study Type: interventional
• Target: 55
• Locations: 1 country
• Sites: 1

Brief Summary

Using of H - test in identifying the sexual behavior of the human.

Conditions

Sexual Behavior; Sexual Orientation Conflict Disorder; Sexual Arousal Disorder; Sexual Orientation; Sexual; Orientation, Relationship Disorder

Outcome Measures

Primary Outcomes (1)

• 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

Study Arms (2)

Hashim Talib Hashim

OTHER

It is a video with +18 different contents to know the effect of much video than the others.

Diagnostic Test: H - Test

Mustafa Ahmed Ramadhan

EXPERIMENTAL

Is is an assessment of the vital signs among the participants and the change with the showing of videos.

Diagnostic Test: H - Test

Interventions

H - Test DIAGNOSTIC_TEST

Showing different videos for a sexual stimulus and monitor the vitals of each participants to measure any changes can occur with each video.

Also known as: Sexual desire test, Sexual health test

Hashim Talib Hashim; Mustafa Ahmed Ramadhan

Eligibility Criteria

• Age: 20 Years - 60 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64)

You may qualify if:

• All the people can be included

You may not qualify if:

• Have a psychological disorder
• Have a sexual disorder

Sponsors & Collaborators

• University of Baghdad: lead

Study Sites (1)

No name

Nasiriyah, Thi Qar, 64001, Iraq

Location

MeSH Terms

Conditions

Sexual Behavior; Sexual Dysfunctions, Psychological; Coitus; Orientation, Spatial

Condition Hierarchy (Ancestors)

Behavior; Mental Disorders; Spatial Behavior

Study Officials

• Talib Manea, MD

  University of Thi-Qar

  STUDY CHAIR

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: DOUBLE
• Who Masked: PARTICIPANT, CARE PROVIDER
• Purpose: DIAGNOSTIC
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Clinical researcher

Study Record Dates

• First Submitted: November 28, 2020
• First Posted: December 17, 2020
• Study Start: December 11, 2020
• Primary Completion: December 25, 2020
• Study Completion: December 26, 2020
• Last Updated: November 1, 2022

Record last verified: 2022-10

Data Sharing

• IPD Sharing: Will share
• Shared Documents: STUDY PROTOCOL, SAP, ICF, CSR, ANALYTIC CODE
• Time Frame: They will be available in three months and for six months.
• Access Criteria: They will shared on drive

Locations

IR (1)