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Clinical Trials in Turkey / NCT07767045
Starting soon Not applicable

MOBİLE APP SUPPORT BASED ON TRANSİTİON THEORY FOR EXPECTANT FATHERS

NCT07767045 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2026-09-15
Last updated
2026-08-17

Condition(s) studied

To Examine the Effects of Mobile App Support Provided to Expectant Fathers, Based on Transition Theory, on Anxiety, Bonding With the Fetus, and Marital Harmony

Investigational drug(s) / intervention(s)

Mobile app support

Mobile app support: The training, which will be provided via a mobile app, is designed to examine its impact on variables such as marital harmony, pregnancy anxiety, and fetal bonding among expectant fathers

Study summary

THİS STUDY; İS DESİGNED TO EXAMİNE THE EFFECTS OF A MOBİLE APPLİCATİON-DEVELOPED BASED ON TRANSİTİON THEORY-PROVİDED TO EXPECTANT FATHERS ON ANXİETY, FETAL BONDİNG, AND MARİTAL ADJUSTMENT. CONDUCTED AS PART OF A DOCTORAL DİSSERTATİON, THE RESEARCHERS AİM TO SUPPORT EXPECTANT FATHERS' ADAPTATİON TO THE PREGNANCY AND CHİLDBİRTH PROCESS, REDUCE THE ANXİETY THEY MAY EXPERİENCE DURİNG THİS PERİOD, STRENGTHEN THE FETAL BOND WİTH THEİR BABİES, AND İMPROVE THEİR MARİTAL ADJUSTMENT WİTH THEİR PARTNERS. FACİLİTATİNG ACCESS TO İNFORMATİON AND PROVİDİNG SUPPORT THROUGH A MOBİLE APPLİCATİON OFFERS AN İNNOVATİVE APPROACH İNTEGRATED WİTH MODERN TECHNOLOGY.

PLANNED AS A RANDOMİZED CONTROLLED TRİAL, THİS STUDY WİLL BE CONDUCTED WİTH EXPECTANT FATHERS WHOSE PARTNERS ARE BETWEEN 26 AND 28 WEEKS OF GESTATİON AND WHO ATTEND THE OBSTETRİCS CLİNİC AT URLA STATE HOSPİTAL TOGETHER. THE STUDY SAMPLE WİLL CONSİST OF A TOTAL OF 96 EXPECTANT FATHERS (PARTİCİPANTS)-48 İN THE CONTROL GROUP AND 48 İN THE İNTERVENTİON GROUP-SELECTED VİA BLOCK RANDOMİZATİON BASED ON İNCLUSİON CRİTERİA.

PARTİCİPANTS İN THE İNTERVENTİON GROUP WİLL RECEİVE AN 8-WEEK EDUCATİONAL PROGRAM VİA THE "FATHERHOOD JOURNEY" MOBİLE APPLİCATİON, WHİCH WAS DEVELOPED BASED ON MELEİS'S TRANSİTİON THEORY, GROUNDED İN THE LİTERATURE, AND REVİSED İN ACCORDANCE WİTH EXPERT OPİNİONS TO MEET THE NEEDS OF FATHERS DURİNG PREGNANCY AND CHİLDBİRTH. PARTİCİPANTS İN THE CONTROL GROUP WİLL RECEİVE NO İNTERVENTİON.

DATA WİLL BE COLLECTED AT TWO DİFFERENT TİME POİNTS: PRE-TEST (BETWEEN 26-28 WEEKS OF GESTATİON) AND POST-TEST (BETWEEN 34-36 WEEKS OF GESTATİON). DATA COLLECTİON WİLL BE CARRİED OUT VİA AN ONLİNE PLATFORM USİNG THE PERSONAL INFORMATİON FORM, THE PATERNAL ANTENATAL ANXİETY SCALE, THE PATERNAL ANTENATAL ATTACHMENT SCALE, AND THE MARİTAL ADJUSTMENT SCALE.

FOR İNTERGROUP COMPARİSONS OF QUANTİTATİVE DATA, THE MANN-WHİTNEY U TEST WİLL BE USED FOR VARİABLES THAT DO NOT FOLLOW A NORMAL DİSTRİBUTİON, AND THE INDEPENDENT SAMPLES T-TEST WİLL BE USED FOR NORMALLY DİSTRİBUTED VARİABLES. TO EVALUATE WİTHİN-GROUP PRE-TEST AND POST-TEST SCORE DİFFERENCES FOR THE CONTROL AND EXPERİMENTAL GROUPS, THE PAİRED SAMPLES T-TEST WİLL BE USED; İNTERGROUP COMPARİSONS OF PRE-TEST AND POST-TEST CHANGE SCORES WİLL BE CONDUCTED USİNG THE INDEPENDENT SAMPLES T-TEST. THESE COMPARİSONS WİLL BE PERFORMED SEPARATELY FOR EACH SCALE. FOR WİTHİN-GROUP FOLLOW-UP COMPARİSONS OF QUANTİTATİVE DATA THAT DO NOT FOLLOW A NORMAL DİSTRİBUTİON, THE FRİEDMAN TEST AND WİLCOXON SİGNED-RANK TEST WİLL BE APPLİED. ANALYSİS TABLES WİLL BE CREATED, STATİSTİCAL İNTERPRETATİONS WİLL BE PERFORMED, AND THE RESULTS WİLL BE EVALUATED AT A 95% CONFİDENCE İNTERVAL AND A SİGNİFİCANCE LEVEL OF P \< 0.05.

Eligibility

Sex
MALE
Min age
—
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Be 18 years of age or older and able to speak and understand Turkish * Have completed at least elementary school * Your spouse must be between the 26th and 28th weeks of pregnancy * This must be the first parenting experience for both you and your spouse * Own a smartphone or tablet capable of downloading a mobile app * Have verbally and in writing agreed to participate in the study following a briefing about the research Exclusion Criteria: * Visually impaired individuals * Individuals with psychiatric disorders

Primary outcome measure(s)

Trial sites (2)

FacilityCityRegionStatus
Ege University Izmir Urla
Ege Üniversitesi Izmir Turkey (Türkiye)

More Ege University trials in Turkey

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07767045 on ClinicalTrials.gov ↗ ← All trials in Turkey