ClinicalTrials.gg
RecruitingNCT07599319Updated May 20, 2026

Avatar-Based Education and Counseling for Spousal Support During Menopause

An interventional study of Avatar-supported menopause education and counseling program in Menopause, sponsored by Eskisehir Osmangazi University. Recruiting at 1 site in Turkey (Türkiye). Open to participants aged 45 Years to 60 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-05-20.

Sponsored by Eskisehir Osmangazi University · Not applicable, Interventional, and Supportive care

From the registry’s dates

  • Registered 9 months after the study started (first participant enrolled Jul 2025, registered Apr 2026).
  • Started Jul 2025; still recruiting 1 year 3 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
280
Allocation
Randomized
Ages
45 Years to 60 Years
Sex
All
01

Study summary

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.

Read the detailed description

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.

02

Conditions studied

  • Menopause

Keywords

  • Spousal Support
  • Education
  • Menopause Education
  • Counseling
  • Avatar-Based Intervention
03

In context

Lead sponsor

Eskisehir Osmangazi University is the lead sponsor of 153 studies on the registry; 27 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
45 Years to 60 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Women aged between 45 and 60 years
  • Being in the menopausal period
  • Married and living with their spouse
  • Able to speak, read, and write in Turkish
  • Able to communicate effectively
  • Willing to participate in the study
  • Having a spouse who is willing to participate
  • Spouses who have internet access and are able to use digital devices

Exclusion criteria

Exclusion Criteria:

  • Women or their spouses with uncontrolled psychiatric disorders requiring treatment
  • Women whose spouses have serious physical or mental health problems that may prevent providing support
  • Women who experienced early menopause (before age 45)
  • Couples who are married but not living together
  • Women and their spouses who participated in the first (qualitative) phase of the study
05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
280 participants (estimated)

Study arms

  • Experimental
    Intervention Group

    Participants will receive a 4-session avatar-based education and counseling program delivered online.

    Other: Avatar-supported menopause education and counseling program

  • No intervention
    Control Group

    Participants will receive routine care without additional intervention.

Interventions

  • OtherAvatar-supported menopause education and counseling program

    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.

06

What researchers measure

Primary outcomes

  1. Change in Spousal Support Level Measured by the Menopause Spousal Support Scale

    Spousal support will be assessed using the Menopause Spousal Support Scale. Total scores will be calculated and compared between groups.

    Time frame: Baseline and 3 months after intervention

Secondary outcomes

  1. Change in Menopause Knowledge Level Measured by the Menopause Knowledge Questionnaire

    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.

    Time frame: Baseline and immediately after intervention

07

Study locations

1 of 1 sites recruiting
  • Bursa Osmangazi Geçit Aile Sağlığı Merkezi
    Bursa, Turkey (Türkiye)
    Recruiting
    • 26 Nolu Geçit Aile Sağlığı Merkezi Aile Sağlığı Merkezi · Contactebefatmaozkar@gmail.com · +905058256967
    • Fatma Özkar · Sub investigator
    • Nebahat Özerdoğan · Principal investigator
08

References and documents

Individual participant data

Plan to share: No — Data collection for the study has not yet actively begun.

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on May 20, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07599319
Responsible party
FATMA ÖZKAR (Midwife, Eskisehir Osmangazi University) — Principal investigator
First posted
May 20, 2026
Start date
Jul 15, 2025
Primary completion
Dec 15, 2026 (estimated)
Completion
Mar 15, 2027 (estimated)
Last update
May 20, 2026

Study contacts

Fatma Özkar
Contact
ebefatmaozkar@gmail.com
+905058256967
Nebahat Özerdoğan
Contact
ozerdogannebahat@gmail.com
+905442395854

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Interested in this study?

Eligibility is decided by the study team. Share this record with your doctor or contact the team directly.

Contact study team

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion