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).
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
- Type of treatment
- Lifestyle or therapy programme
- 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.
Ümran Oskay, PhD, Prof. contact
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
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.
- Conditions
- Preconception Period
- 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 group | Role | What they receive |
|---|---|---|
| Intervention Group | Experimental | Women 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 Group | Active comparator | Women 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.
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)
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
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
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.
- First posted12 Dec 2025
- Study start1 Jan 2026 (estimated)
- Primary completion1 Sep 2026 (estimated)
- Study completion30 Dec 2026 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Preconception PeriodStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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)
Sponsor and investigators
- Lead sponsor
- Selinay Aktaş Demir
- Sponsor type
- University, hospital or other
- Responsible party
- Sponsor-investigator, Selinay Aktaş Demir, Atlas University
- Investigators
- Selinay Aktaş Demir, RN, PhD Student, Principal investigator, Atlas ÜniversitesiÜmran Oskay, PhD, Prof., Study chair, Istanbul University - Cerrahpasa
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
Study at a glance
From the registry record, last updated by the sponsor on 12 Dec 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- The Impact of a Mobile Application-based Support and Counseling Program on Women's Knowledge, Attitudes and Self-efficacy in the Preconceptional Period
- ClinicalTrials.gov ID
- NCT07279857
- Acronym / sponsor ID
- ATLASU-AKTASDEMIR-001
- Conditions
- Preconception Period
- Keywords
- Preconception Care, Preconception Counseling, Mobile Health (mHealth), Digital Health Intervention, Women's Health, Reproductive Health, Self-Efficacy
- Study type
- Interventional
- Recruitment status
- Not yet recruiting
- Enrolment
- 110 participants (estimated)
- Lead sponsor
- Selinay Aktaş DemirUniversity, hospital or other
- Study start
- 1 Jan 2026 (estimated)
- Primary completion
- 1 Sep 2026 (estimated)
- Study completion
- 30 Dec 2026 (estimated)
- First posted
- 12 Dec 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
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.
Study design
- Primary purpose
- Health services research
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- Single blind (participant)
- Number of arms
- 2
- 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.
| Arm | Type | Receives |
|---|---|---|
| Intervention Group | Experimental | Behavioral: Mobile Application-Based Preconception Counseling ProgramWomen receive a four-week mobile application-based preconception counseling program including weekly modules, reminders, and messaging support. |
| Control Group | Active comparator | Behavioral: Standard Preconception Information BookletWomen receive a standard preconception information booklet containing guideline-based educational content. |
Who may qualify
- Ages
- 18 to 49 years
- Sex
- Female only
- Healthy volunteers
- Accepted
- Age groups
- Adult
Key inclusion criteria (6 listed)
- 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.
Key exclusion criteria (6 listed)
- 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.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Mobile Application-Based Preconception Counseling ProgramA structured digital education and counseling program delivered through a mobile application, including weekly modules, reminders, and in-app messaging support. | Behavioural | Intervention Group |
| Standard Preconception Information BookletA printed booklet providing standard guideline-based preconception information without digital follow-up. | Behavioural | Control Group |
Primary outcome
Change in Preconception Knowledge Score
Time frame: Baseline, Week 4, Week 12
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.
3 secondary outcomes
Change in Preconception Attitudes Score
Time frame: Baseline, Week 4, Week 12
Change in Self-Efficacy Score
Time frame: Baseline, Week 4, Week 12
Mobile Application Usability Score
Time frame: Week 4
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 12 Dec 2025.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Ümran Oskay, PhD, Prof. contact
Selinay Aktaş Demir, RN, PhD Student principal investigator
Atlas Üniversitesi
Ümran Oskay, PhD, Prof. study chair
Istanbul University - Cerrahpasa
1 site in 1 country: see every site and its status.
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.