CompletedNot Applicable

Feeding Readiness and Oral Feeding Success in Preterm Infants

Turkey (Türkiye)60 participantsStarted 2020-06-01

Plain-language summary

To examine the effects of sensorimotor interventions applied to in preterm infants on readiness for feeding and oral feeding success.

Who can participate

Age range

30 Weeks – 33 Weeks

Sex

ALL

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: * The mother's milk * Preterm babies with a gestational age of 30-33 weeks * No facial deformity, * No respiratory, cardiovascular, gastrointestinal and neurological disorders or syndromes that would prevent or complicate oral feeding, * No need for oxygen support, * There will be preterm infants who are not fed orally, but who are started with tube (Orogastric) feeding. Exclusion Criteria: * Transferred to another center during the research, * Unexpected complication development during the research, * Occurrence of a pathology that will prevent or complicate oral feeding, * In cases where there is no voluntary consent of the parent * The mother is Covid positive

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

Oral Feeding Readiness

Timeframe: 10 days change in T-POFRAS (feeding readiness) after sensorimotor intervention.

Trial details

NCT IDNCT04946045

SponsorPamukkale University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2020-06-01

View on ClinicalTrials.gov More Preterm trials

Who can participate

Age range

30 Weeks – 33 Weeks

Sex

ALL

See this in plain English?

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