Bursa Osmangazi Geçit Aile Sağlığı Merkezi
Bursa, Turkey (Türkiye)
Location status: Recruiting
Location contact
26 Nolu Geçit Aile Sağlığı Merkezi Aile Sağlığı Merkezi
CONTACT
Fatma Özkar
SUB_INVESTIGATOR
Nebahat Özerdoğan
PRINCIPAL_INVESTIGATOR
NCT Number: NCT07599319
This study aims to evaluate the effectiveness of an avatar-based education and counseling program in increasing spousal support during menopause. The study will include menopausal women and their spouses. Participants will be assigned to intervention and control groups. The intervention group will receive a structured online avatar-based education and counseling program, while the control group will receive routine care. Outcomes will be assessed before and after the intervention, as well as during follow-up periods.
Interested in participating?
Request Info45 year–60 year
All sexes
Interventional
Not applicable
Bursa, Turkey (Türkiye)
Location status: Recruiting
26 Nolu Geçit Aile Sağlığı Merkezi Aile Sağlığı Merkezi
CONTACT
Fatma Özkar
SUB_INVESTIGATOR
Nebahat Özerdoğan
PRINCIPAL_INVESTIGATOR
This study aims to evaluate the effectiveness of an avatar-based education and counseling program designed to increase spousal support during menopause. The study will be conducted using a randomized controlled experimental design.
Participants will consist of menopausal women and their spouses. Eligible couples will be randomly assigned to either an intervention group or a control group. The intervention group will receive a structured avatar-based education and counseling program delivered online in four sessions, while the control group will receive routine care without additional intervention.
The intervention program focuses on improving knowledge about menopause, enhancing communication and empathy skills, and promoting supportive behaviors among spouses. The program is developed based on prior qualitative findings and relevant literature.
Data will be collected at baseline (pre-test), immediately after the intervention (post-test), and during follow-up assessments at 1, 2, and 3 months. Primary and secondary outcomes will be evaluated using validated measurement tools.
The effectiveness of the intervention will be assessed by comparing changes in outcomes between the intervention and control groups over time.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
The primary intervention of the study, the education and counseling program, will be delivered to participants assigned to two groups through four online sessions. During the sessions, an avatar will be used to present the educational and counseling content in order to enable participants to ask questions more comfortably and express themselves, particularly on issues related to their private lives. In addition, the educational materials will be shared with participants' mobile phones via WhatsApp, and participants will be able to ask questions through WhatsApp communication.
Time frame: Baseline and 3 months after intervention
Spousal support will be assessed using the Menopause Spousal Support Scale. Total scores will be calculated and compared between groups.
Time frame: Baseline and immediately after intervention
Menopause knowledge levels of spouses will be assessed using the Menopause Knowledge Questionnaire. Total scores will be calculated and compared before and after the intervention.
Contact information is provided by the study sponsor or research team.
Fatma Özkar
CONTACT
Nebahat Özerdoğan
CONTACT
Eskisehir Osmangazi University
Other
Effect of an Avatar-Based Education and Counseling Program on Spousal Support During Menopause
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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