AzTrials
AzTrials

Preconception PeriodNCT07279857

The Impact of a Mobile Application-based Support and Counseling Program on Women's Knowledge, Attitudes and Self-efficacy in the Preconceptional Period

A study testing Mobile Application-Based Preconception Counseling Program and Standard Preconception Information Booklet in people with Preconception Period, run by Selinay Aktaş Demir at 1 site in Turkey (Türkiye).

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
Search all trials

Trial summary

This randomized controlled trial aims to evaluate the effect of a mobile application-based support and counseling program on women in the preconception period. The study includes women aged 18 to 49 who plan to conceive within two years and meet the eligibility criteria. Read more about this study

Who is it for?
Ages 18 to 49 years, women onlyHealthy volunteers can take part
Conditions the study is for
Preconception Period
What is being tested?
Mobile Application-Based Preconception Counseling Program and Standard Preconception Information Booklet
Could I receive a placebo?
No, everyone receives an active treatment
How many people
110 participants
Where
1 siteTurkey (Türkiye)
Study dates
1 Jan 2026to 30 Dec 2026
Phase
Interventional
Are there results?
Not yet: the study is under way

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 49 years
  • Women only
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Women aged 18 to 49 years.
  • In the preconception period and planning to conceive within the next two years.
  • Never been pregnant.
  • Able to read and understand Turkish.
  • Having a smartphone and internet access.
  • Willing to participate and provide informed consent.

Who cannot join

  • Currently pregnant.
  • Having a diagnosed psychiatric disorder that may interfere with participation.
  • Previous participation in structured preconception counseling or training.
  • Being a health professional or a student in a health-related field.
  • Inability to use a mobile application due to cognitive, visual, or physical limitations.
  • Participation in another ongoing research study.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Selinay Aktaş Demir, RN, PhD Student contact

+905387307340

selinayaktas7@outlook.com

Ümran Oskay, PhD, Prof. contact

umran.oskay@iuc.edu.tr

Turkey (Türkiye)1 site
  • Bayrampaşa İlçe Sağlık Müdürlüğü Aile Sağlığı Merkezleri

    Istanbul

    Selinay Aktaş Demir, Phd Student, RN, +90 538 730 7340, selinayaktas7@outlook.com

    Ümran Oskay, PhD, Prof., +90 212 414 30 00, umran.oskay@iuc.edu.tr

Other trials in Turkey (Türkiye)

About this study

This randomized controlled trial aims to evaluate the effect of a mobile application-based support and counseling program on women in the preconception period. The study includes women aged 18 to 49 who plan to conceive within two years and meet the eligibility criteria. Participants are randomly assigned to an intervention group receiving structured preconception counseling through a mobile application or a control group receiving standard information via a booklet. The intervention consists of weekly educational modules delivered over four weeks, followed by follow-up assessments at 4 and 12 weeks. Primary outcomes include changes in preconception knowledge, attitudes, and self-efficacy. The study seeks to determine whether mobile health-based counseling enhances preconception preparedness compared with standard information.

Read the detailed description

This randomized controlled trial investigates the effectiveness of a structured mobile application-based support and counseling program designed for women in the preconception period. Preconception care plays a critical role in improving maternal and fetal outcomes by addressing biomedical, behavioral, and psychosocial risk factors before pregnancy. Despite increasing global use of mobile health technologies, there is no comprehensive mobile application-based preconception counseling program developed and evaluated in Türkiye. This study aims to address this gap by implementing a digitally delivered intervention grounded in established guidelines from the CDC and WHO.

The study includes women aged 18 to 49 who are in the preconception period, have never been pregnant, plan to conceive within two years, can use a smartphone, and have internet access. Women who are currently pregnant, health professionals, those with diagnosed psychiatric conditions, or those who have previously received preconception counseling are excluded. A total of 110 eligible participants are enrolled and randomly assigned to intervention or control groups using a simple randomization procedure generated through an online randomization system (random.org). Because the intervention requires participant engagement with content, the study is conducted as a single-blind design, with participants unaware of their group allocation.

The intervention group receives a four-week mobile application-based counseling program developed using the ADDIE (Analysis, Design, Development, Implementation, Evaluation) instructional design model. The application delivers weekly modules covering preconception care concepts, risk assessment, nutrition, supplementation, physical activity, immunization, sexually transmitted infections, environmental exposures, oral and dental health, psychosocial well-being, reproductive planning, and lifestyle behaviors such as tobacco, alcohol, and medication use. Each module includes structured educational content, reminders, and communication tools enabling researcher-participant interaction. Participants receive weekly follow-ups via messaging to identify difficulties, support adherence, and address questions. The application also includes built-in progress tracking and notification functions.

The control group receives a printed booklet containing standardized preconception information aligned with the topics covered in the intervention modules. Control group participants do not receive digital follow-up but participate in the same assessment schedule as the intervention group.

Data are collected at baseline, at week 4, and at week 12 after the start of the study. Instruments include: a descriptive information form, the Preconception Knowledge and Attitudes Scale, the General Self-Efficacy Scale, a preconception risk assessment form, and for the intervention group, the Mobile Application Usability Scale. Baseline assessments include sociodemographic characteristics, lifestyle indicators, and preconception risk factors. Week 4 assessments measure short-term changes in knowledge, attitudes, and self-efficacy. Week 12 assessments evaluate persistence of intervention effects and longer-term retention of gains.

The primary outcomes are changes in preconception knowledge, attitudes, and self-efficacy. Secondary outcomes include user-reported usability and acceptability of the mobile application. The study evaluates whether a mobile health-based digital counseling approach provides measurable benefits beyond conventional booklet-based information and whether its effects persist beyond the immediate intervention period.

The findings are expected to contribute to the development of evidence-based, scalable, digital preconception care strategies appropriate for primary health care settings, particularly in contexts where accessibility, continuity, and standardization of preconception counseling services are limited.

Being tested
Mobile Application-Based Preconception Counseling Program, Standard Preconception Information Booklet
Keywords
Preconception Care, Preconception Counseling, Mobile Health (mHealth), Digital Health Intervention, Women's Health, Reproductive Health, Self-Efficacy

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Mobile Application-Based Preconception Counseling ProgramBehavioural

    A structured digital education and counseling program delivered through a mobile application, including weekly modules, reminders, and in-app messaging support.

  • Standard Preconception Information BookletBehavioural

    A printed booklet providing standard guideline-based preconception information without digital follow-up.

Study groups in NCT07279857
Study groupRoleWhat they receive
Intervention GroupExperimentalWomen receive a four-week mobile application-based preconception counseling program including weekly modules, reminders, and messaging support.
Receives: Behavioral: Mobile Application-Based Preconception Counseling Program
Control GroupActive comparatorWomen receive a standard preconception information booklet containing guideline-based educational content.
Receives: Behavioral: Standard Preconception Information Booklet

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change in Preconception Knowledge Score

    Preconception knowledge is assessed using the Preconception Knowledge and Attitudes Scale. The primary outcome is the change in total knowledge score from baseline to week 4 and week 12. Higher scores indicate higher preconception knowledge.

    Measured: Baseline, Week 4, Week 12

Secondary outcomes (3)
  1. Change in Preconception Attitudes Score

    Attitudes toward preconception health are measured using the attitude subscale of the Preconception Knowledge and Attitudes Scale. Change in attitude score is evaluated between baseline, week 4, and week 12.

    Measured: Baseline, Week 4, Week 12

  2. Change in Self-Efficacy Score

    Self-efficacy is assessed using the General Self-Efficacy Scale. The outcome measure is the change in total self-efficacy score across baseline, week 4, and week 12.

    Measured: Baseline, Week 4, Week 12

  3. Mobile Application Usability Score

    Usability of the mobile application is assessed using a validated usability scale. Usability is measured at week 4 among participants in the intervention group.

    Measured: Week 4

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted12 Dec 2025
  2. Study start1 Jan 2026 (estimated)
  3. Primary completion1 Sep 2026 (estimated)
  4. Study completion30 Dec 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Health services research
Allocation
Randomised
Intervention model
Parallel groups
Model description
Participants are randomized into two parallel groups: a mobile application-based counseling intervention group and a standard-information control group. Both groups receive their assigned intervention simultaneously, and outcomes are measured at baseline, week 4, and week 12.
Masking
Single blind
Who is masked
Participant
Enrolment
110 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07279857
Sponsor's protocol ID
ATLASU-AKTASDEMIR-001
Status last verified
Dec 2025
First submitted
1 Dec 2025
Last updated
12 Dec 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Mobile Application-Based Preconception Counseling Program and Standard Preconception Information Booklet in people with Preconception Period, run by Selinay Aktaş Demir at 1 site in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 6 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: opening soon, as of the sponsor's last update on 12 Dec 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

This study is still under way. Results are not available in the source record yet.

How can a doctor refer a patient or contact the research team?

Contact Selinay Aktaş Demir, RN, PhD Student (+905387307340, selinayaktas7@outlook.com), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change in Preconception Knowledge Score (time frame: Baseline, Week 4, Week 12). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 12 Dec 2025.

Free account

Keep searching with a free account

You’ve used your 3 free searches for this session. Log in or create a free AzTrials account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in