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Clinical Trials/IRCT20230820059202N1
IRCT20230820059202N1
Not Yet Recruiting
N/A

Design and evaluation the effect of Educational mobile Application on sexual function and sexual quality of life in women with endometriosis under medical treatment

Shahid Beheshti University of Medical Sciences0 sites100 target enrollmentTBD
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Overview

Phase
N/A
Intervention
Not specified
Conditions
Not specified
Sponsor
Shahid Beheshti University of Medical Sciences
Enrollment
100
Status
Not Yet Recruiting
Last Updated
last year
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

Overview

Brief Summary

No summary available.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
last year
Study Type
Interventional
Sex
Female

Investigators

Eligibility Criteria

Inclusion Criteria

  • •Endometriosis has been diagnosed in them by a gynecologist through ultrasound
  • •To be sexually active during the last month
  • •There is no known infertility problem in any of the couples
  • •There should be no known sexual dysfunction in the male partner such as erectile dysfunction, ejaculation disorder
  • •Does not have any known underlying diseases such as mental illness, cardiovascular disease, kidney disease, diabetes, excretory disease, pelvic inflammatory disease and other women's diseases
  • •Absence of urinary tract infection, vaginitis, cervical inflammation, active wounds or genital lesions that interfere with sexual intercourse, or a history of sexual assault
  • •Women have not used any drugs affecting sexual function such as antidepressants, beta blockers, antihistamines, antipsychotics, benzodiazepines, antiepileptic drugs
  • •Couples should not consume cigarettes, alcohol and drugs
  • •Not experiencing stressful events (death of a child or a close relative, severe illness of a close relative, imprisonment of a family member, depression, etc.) in the last 3 months
  • •The couple has not taken various sex education classes or courses

Exclusion Criteria

  • •Failure to fully complete research questionnaires

Outcomes

Primary Outcomes

Not specified

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