Not Yet RecruitingNot Applicable

Developmental Support Program: A Intervention Study

60 participantsStarted 2026-09-01

Plain-language summary

This study aims to evaluate the effectiveness of an online video-based developmental support program for parents of children aged 1-3 years receiving care at a Family Health Center. Approximately 60 parents will be randomly assigned to either an intervention group, which will receive a four-week online developmental support program, or a control group, which will continue to receive usual healthcare services. Data will be collected at baseline, two weeks after the intervention, and at one- and three-month follow-up assessments. The study will examine the effects of the online video-based developmental support program on parents' attitudes toward child development, developmental awareness, parenting self-efficacy, and the quality of the home environment that supports child development.

Who can participate

Age range

15 Years – 65 Years

Sex

FEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Parents with children aged 12-36 months * Children with a percentile value between the 3rd and 97th percentile * Able to speak and understand Turkish * No previous participation in a similar program * Having internet access and the ability to use a computer/laptop, tablet, or smartphone * At least primary school graduates * Able to read and comprehend written information * Willing to participate in the study Exclusion Criteria: * Adolescent parents * Parents of children with congenital anomalies, chronic diseases, or a history of prematurity * Individuals with a diagnosed mental health disorder

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

0-6 Years Psychosocial Developmental Attitudes Scale

Timeframe: From enrollment to 3 months after completion of the intervention

Interpersonal Mindfulness in Parenting Questionnaire

Timeframe: From enrollment to the end of the 3-month follow-up period after the interventio

Parenting Self-Efficacy Scale

Timeframe: From enrollment to the end of the 3-month follow-up period after the intervention

Infant-Toddler Home Observation for Measurement of the Environment (IT-HOME) Inventory

Timeframe: From enrollment to the end of the 3-month follow-up period after the intervention

Trial details

NCT IDNCT07656272

SponsorTC Erciyes University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2026-12-31

Contact for this trial

Pınar Ateş, Registered Nurse

+90 507 786 81 91 pinarates505@gmail.com

View on ClinicalTrials.gov More Development and Health trials

Plain-language summary

Who can participate

Age range

15 Years – 65 Years

Sex

FEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

What they're measuring

0-6 Years Psychosocial Developmental Attitudes Scale

Timeframe: From enrollment to 3 months after completion of the intervention

Interpersonal Mindfulness in Parenting Questionnaire

Timeframe: From enrollment to the end of the 3-month follow-up period after the interventio

Parenting Self-Efficacy Scale

Timeframe: From enrollment to the end of the 3-month follow-up period after the intervention

Infant-Toddler Home Observation for Measurement of the Environment (IT-HOME) Inventory

Timeframe: From enrollment to the end of the 3-month follow-up period after the intervention