Sexual Health Literacy Scale
SHLS
Development of the Sexual Health Literacy Scale
1 other identifier
observational
400
1 country
1
Brief Summary
According to the World Health Organization, sexual health is a state of well-being related to sexuality as a whole, not just the absence of disease or dysfunction or disability. sexual health; It requires a positive and respectful attitude, free from sexual coercion and discrimination, free of violence, enjoyable and safe experiences. It obliges the respect, protection and fulfillment of the sexual rights of every individual. sexual health; includes a safe and respectful framework free from violence and discrimination; it covers not only the reproductive period, but every age period; different sexual identities and forms of sexual expression, as well as livable and critical gender values, roles, expectations and power dynamics. Insufficient information, difficult access to health services and lack of a guiding structure; It negatively affects young individuals' ability to take responsible decisions with good knowledge about sexuality during their sexual development. Information is obtained from channels where erroneous and incorrect information transfer is intense, and the ways of accessing this information play an important role in the spread of sexual myths in society. Based on all these reasons; This study aimed to develop the Sexual Health Literacy Scale.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Mar 2024
Shorter than P25 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
April 5, 2023
CompletedFirst Posted
Study publicly available on registry
April 20, 2023
CompletedStudy Start
First participant enrolled
March 4, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 30, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
October 30, 2024
CompletedNovember 20, 2024
November 1, 2024
3 months
April 5, 2023
November 18, 2024
Conditions
Outcome Measures
Primary Outcomes (2)
scale development
The data will be collected with the online data collection tool created by the researchers through the software called google forms. During data collection, the e-mail address of the researchers will be indicated on the form so that the questions of the participants can be answered by the researchers. You will be informed that filling out the data collection form will take an average of 10 minutes for each participant. In addition, in order to evaluate the test-retest reliability of the scale, data collection tools will be sent to at least 30 randomly selected individuals from the sample two weeks after the first data collection.
3 month
test-retest reliability of the scale
In order to evaluate the test-retest reliability of the scale, data collection tools will be sent to at least 30 randomly selected individuals from the sample two weeks after the first data collection. Therefore, after the pre-application, the scale will be applied to 400 people within the scope of the calculated sample, and then, two weeks later, at least 50 people will be re-applied from the individuals to whom the same scale was applied.
Retest( later 2 weeks)
Interventions
The scale development process generally consists of three stages as item production, theoretical analysis and psychometric analysis. The researcher provides theoretical support to the item pool during item production. In the theoretical analysis stage, the content validity of the new scale is evaluated and the first item pool is ensured to reflect the desired structure. In the final stage of the psychometric analysis, the researcher evaluates whether the new scale establishes validity and reliability.
Eligibility Criteria
It is very difficult to determine what kind of universe individuals over the age of 18 create and to reach the representative group even if it is determined. For this reason, rather than the criterion of representing the universe, it was based on creating a heterogeneous sample group by considering various age groups in a "fit for purpose" way. In this direction, the "snowball sampling" technique, which is one of the non-random sampling types, was preferred. Snowball sampling is a sampling method used in cases where it is difficult to reach the desired population and sample, including quantitative research, especially qualitative research, and the desired sampling frame does not include a large number of sample individuals.
You may qualify if:
- Individuals over the age of 18 who are willing to participate in the study, without psychiatric illness,
- No physical or mental disability
- Able to speak and understand Turkish.
You may not qualify if:
- Not willing to participate in the study, with psychiatric illness,
- Physically and mentally handicapped
- years and under,
- Does not speak Turkish
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Nurdan Demircilead
Study Sites (1)
Marmara University
Istanbul, 34854, Turkey (Türkiye)
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Rüveyda Ölmez Yalazı, PhDc
Marmara University
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- CROSS SECTIONAL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Prof
Study Record Dates
First Submitted
April 5, 2023
First Posted
April 20, 2023
Study Start
March 4, 2024
Primary Completion
May 30, 2024
Study Completion
October 30, 2024
Last Updated
November 20, 2024
Record last verified: 2024-11
Data Sharing
- IPD Sharing
- Will not share