Online and Mobile Support Program and Fertility

ConditionsInfertility Stress

Trial statusNot yet recruiting

Trial phaseNot applicable

Trial typeInterventional

Biological sexFemale

AgeNot listed

SponsorDokuz Eylul University

About this trial

Our study is designed as a randomized controlled experimental study with a pre-test and post-test control group to determine the effects of online fertility preparation classes and fertility mobile application support, based on the Philosophy of Hypnofertility and Pender's Health Promotion Model, on infertile women's fertility readiness, fertility self-efficacy, lifestyle, and pregnancy outcomes.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Having been diagnosed with primary infertility,

Having been diagnosed with female, male factor and unexplained infertility,

Cycles where fresh embryos will be applied

Having In Vitro Fertilization (IVF) treatment,

Disqualifiers

Cycles to be performed with frozen embryos

Having any psychiatric disorder,

Attending less than 80% of the trainings (not attending more than 2 classes) in this case women will be excluded from the study and in order to reach a sufficient sample, institutions will be visited again and cases that meet the sample criteria will be found. Re-randomization will be done among women who meet the criteria

Having any chronic disease for which they are receiving treatment.

Trial design

Design model

Parallel

Treatments tested in this trial

MOBIL AND ONLINE EDUCATION
Other intervention
The intervention group attended synchronous online sessions twice weekly (2 hours) for four weeks before IVF, with the mobile app available from the first session. During IVF cycles, the app provided scheduled educational content, reminders, creation of lifestyle maps, feedback,counseling scheduling, and daily motivational messages based on hypnofertility principles to enhance support.

Treatment groups

128 Participants

are divided into 2 treatment groups

Group A: InterventionExperimental treatment 1 intervention

Group B: ControlNo intervention 0 interventions

Trial outcomes

Primary outcomes

pregnancy outcome

The occurrence of clinical pregnancy after treatment will be evaluated.

Time frame

1 mounth

Secondary outcomes

Fertility Readiness, Self-efficacy, Lifestyle

Fertility Readiness Scale for Women Receiving Fertility Support; A high score indicates strong fertility readiness. The minimum score that can be obtained from the scale is 23, while the maximum score is 115.

Time frame

6 mounth

Other outcomes

Fertility Self Eficacy

The Infertility Self-Efficacy Scale - Short Form (ISSS-SF) scores range from 8 to 32. As the score increases, the perception of self-efficacy is considered to be higher. All statements in the scale are positively worded, and there is no cutoff point for the scale.

Time frame

6 mounth

Healthy Lifestyle Behaviors

The 46-item Scale of Healthy Lifestyle Behaviors in Fertility Development is scored on a 5-point Likert scale, with a minimum score of 46 and a maximum score of 230. An increase in the scale score indicates a higher intensity of healthy lifestyle behaviors among individuals.

Time frame

6 mounth

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Dokuz Eylul University

Lead sponsor

Source ClinicalTrials.gov

This trial is not recruiting at the moment. You can still explore other options: