- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT03303326
Arab American Women's Health Study
Studieöversikt
Detaljerad beskrivning
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).
Studietyp
Inskrivning (Faktisk)
Fas
- Inte tillämpbar
Kontakter och platser
Studieorter
-
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Michigan
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Detroit, Michigan, Förenta staterna, 48201
- Wayne State University
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Deltagandekriterier
Urvalskriterier
Åldrar som är berättigade till studier
Tar emot friska volontärer
Kön som är behöriga för studier
Beskrivning
Inclusion Criteria:
- Arab American or Chaldean
- Female
- Age 18-35
Exclusion Criteria:
- Non-English speaking
Studieplan
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Grundläggande vetenskap
- Tilldelning: Randomiserad
- Interventionsmodell: Parallellt uppdrag
- Maskning: Ingen (Open Label)
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
|---|---|
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Experimentell: Immediate Interview
A 60-minute interview about women's health conducted immediately after baseline questionnaires.
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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.
Andra namn:
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Inget ingripande: Delayed Interview
The interview is conducted after the follow-up questionnaires are completed, rather than after baseline.
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Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
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Patient Health Questionnaire
Tidsram: Change from baseline to 5-week follow-up
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Physical symptoms
|
Change from baseline to 5-week follow-up
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Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
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Brief Symptom Inventory
Tidsram: Change from baseline to 5-week follow-up
|
Psychological symptoms
|
Change from baseline to 5-week follow-up
|
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Satisfaction with Life Scale
Tidsram: Change from baseline to 5-week follow-up
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Satisfaction with life
|
Change from baseline to 5-week follow-up
|
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Sexual Self-Schema Scale
Tidsram: Change from baseline to 5-week follow-up
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Sexual self-schemas
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Change from baseline to 5-week follow-up
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Sexual Self Disclosure Scale (Catania)
Tidsram: Change from baseline to 5-week follow-up
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Self-reported ease or difficulty with disclosing information about sexuality
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Change from baseline to 5-week follow-up
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Sexual Self Disclosure Scale (Herold & Way)
Tidsram: Change from baseline to 5-week follow-up
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Degree of past sexual disclosure
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Change from baseline to 5-week follow-up
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Female Sexual Function Index
Tidsram: Change from baseline to 5-week follow-up
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Female sexual function
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Change from baseline to 5-week follow-up
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Sexual Satisfaction Scale for Women
Tidsram: Change from baseline to 5-week follow-up
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Sexual satisfaction
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Change from baseline to 5-week follow-up
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Samarbetspartners och utredare
Sponsor
Samarbetspartners
Utredare
- Huvudutredare: Mark Lumley, PhD, Wayne State University
Studieavstämningsdatum
Studera stora datum
Studiestart (Faktisk)
Primärt slutförande (Faktisk)
Avslutad studie (Faktisk)
Studieregistreringsdatum
Först inskickad
Först inskickad som uppfyllde QC-kriterierna
Första postat (Faktisk)
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
Senast verifierad
Mer information
Termer relaterade till denna studie
Nyckelord
Andra studie-ID-nummer
- 064917B3E
Plan för individuella deltagardata (IPD)
Planerar du att dela individuella deltagardata (IPD)?
Läkemedels- och apparatinformation, studiedokument
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