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临床试验/NCT07279857
NCT07279857
尚未招募
不适用

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

Selinay Aktaş Demir1 个研究点 分布在 1 个国家目标入组 110 人开始时间: 2026年1月1日最近更新:

概览

阶段
不适用
状态
尚未招募
发起方
Selinay Aktaş Demir
入组人数
110
试验地点
1
主要终点
Change in Preconception Knowledge Score

概览

简要总结

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.

详细描述

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Health Services Research
盲法
Single (Participant)

盲法说明

Participants are blinded to group assignment; the researcher delivering the intervention is not blinded.

入排标准

年龄范围
18 Years 至 49 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • 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.

排除标准

  • 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.

结局指标

主要结局

Change in Preconception Knowledge Score

时间窗: 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.

次要结局

  • Change in Preconception Attitudes Score(Baseline, Week 4, Week 12)
  • Change in Self-Efficacy Score(Baseline, Week 4, Week 12)
  • Mobile Application Usability Score(Week 4)

研究者

发起方
Selinay Aktaş Demir
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Selinay Aktaş Demir

Lecturer, RN, MSc, PhD Student

Atlas University

研究点 (1)

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