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NCT07690969
Mobile Health Support Before Oocyte Pick-Up in Infertile Women
Conditions: Female İnfertility
Sex: Female
Ages: 18 Years – N/A
Healthy volunteers: No
Phase: NA
Enrollment: 60
Sponsor: Istinye University
Location: Medipol MEGA University Hospital Istanbul
Summary
This study aims to evaluate the effect of the OPUCARE system, a structured mobile health application used before oocyte pick-up (OPU), on medication adherence and quality of life in infertile women. The study will also examine the possible effect of the intervention on state anxiety.
Participants will be randomly assigned to either the intervention group or the control group. The intervention group will receive routine clinical care plus the OPUCARE system. The control group will receive routine clinical care and standard written and verbal information provided by the clinic, without mobile health application support.
The intervention period will last approximately 2 weeks, from the start of medication treatment until oocyte pick-up. Medication adherence, quality of life, and state anxiety will be assessed before and after the intervention period.
Eligibility Criteria
Inclusion Criteria:
* Female participants aged 18 years and older
* Diagnosed with primary infertility
* Scheduled to undergo oocyte pick-up (OPU) for the first time
* Newly starting medication treatment during the period before OPU
* Own a smartphone and are able to use basic mobile applications
* Willing to participate in the study and provide written informed consent
Exclusion Criteria:
* Diagnosis of secondary infertility
* Presence of a serious chronic disease that may significantly affect medication adherence and/or quality of life
* Presence of an active serious psychiatric disorder
* Cognitive or physical limitation that prevents use of the mobile application
Source: ClinicalTrials.gov (NCT07690969). StuddyBuddy aggregates publicly available trial information.