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Completed

NCT Number: NCT03303326

Arab American Women's Health Study

This study evaluates how Arab American women's cultural values and sexual health are related to their physical and emotional health. The study will also examine whether engaging in a sexual health interview affects women's physical and emotional health.

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Key information

Age range

18 year–35 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Wayne State University

Detroit, Michigan, 48201, United States

About this study

Sexuality is an important aspect of health, in part because emotional conflicts over sexuality as well as unwanted sexual experiences can impact physical and psychological health; yet no studies have examined sexual health among Arab American women in the U.S. These women face the task of negotiating their heritage culture and the American culture in which they reside. This may result in bicultural identity conflict for some women as they try to negotiate these two identities, which may have implications for sexuality and sexual health due to the two cultures' disparate views on sexuality. Confidential discussion of these sensitive topics with a knowledgeable interviewer may yield beneficial effects.

The overall goal of the current study is to fill the gap in the literature on Arab American sexual health by examining how sexual health is related to physical and psychological health. This will be accomplished using both: a) correlational findings about sexual, physical, and psychological health from information gathered through self-report questionnaires and a 60-minute women's health interview; and b) an experimental test of the effects of the women's health interview on physical and psychological health. A sample of young adult Arab American women will be assessed at baseline via questionnaires for various constructs (sexual attitudes, cultural and religious identity, and physical and mental health), and then randomized to either an immediate or delayed health interview, with a 5-week follow-up reassessment.

It is hypothesized that lower sexual well-being, negative sexual self-schemas, and unwanted sexual experiences will correlate with more somatic and psychological health symptoms and lower satisfaction with life. It is also hypothesized that participants who have the immediate interview will report greater reduction in somatic and psychological symptoms and a greater willingness to discuss sexual health with medical providers compared to participants who are not interviewed (i.e., have a delayed interview after follow-up assessment).

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Arab American or Chaldean
  • Female
  • Age 18-35

Exclusion criteria

  • Non-English speaking

Treatment and study plan

Immediate interview

Behavioral

A women's health interview that obtains information about physical, mental, and sexual health, particularly relatively private sexual health-related attitudes and experiences, as well as conflicts and stress related to sexuality.

Other names: Women's Health Interview

Primary outcomes

  1. Patient Health Questionnaire

    Time frame: Change from baseline to 5-week follow-up

    Physical symptoms

Secondary outcomes

  1. Brief Symptom Inventory

    Time frame: Change from baseline to 5-week follow-up

    Psychological symptoms

  2. Satisfaction with Life Scale

    Time frame: Change from baseline to 5-week follow-up

    Satisfaction with life

  3. Sexual Self-Schema Scale

    Time frame: Change from baseline to 5-week follow-up

    Sexual self-schemas

  4. Sexual Self Disclosure Scale (Catania)

    Time frame: Change from baseline to 5-week follow-up

    Self-reported ease or difficulty with disclosing information about sexuality

  5. Sexual Self Disclosure Scale (Herold & Way)

    Time frame: Change from baseline to 5-week follow-up

    Degree of past sexual disclosure

  6. Female Sexual Function Index

    Time frame: Change from baseline to 5-week follow-up

    Female sexual function

  7. Sexual Satisfaction Scale for Women

    Time frame: Change from baseline to 5-week follow-up

    Sexual satisfaction

Sponsors and collaborators

Lead sponsor

Wayne State University

Other

Collaborators

  • Blue Cross Blue Shield of Michigan Foundation

Registry information

Important dates

Study start
2017
Primary completion
2018
Study completion
2018
First posted
Oct 6, 2017
Registry last updated
Oct 2, 2018

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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