Cot-side Suckometry and Oral Stimulation in Very Preterm Infants: A Pilot Study (STIMPREM)
Early Evolution of Oral Feeding Skills in Very Preterm Infants: Impact of an Oral Stimulation Program Assessed by Cot-side Suckometer
Very preterm infants - born before 32 weeks' gestational age - commonly experience delayed transition to oral feeding due to immature suck-swallow-breathe coordination. This prospective pilot study have two aims: (1) to assess the feasibility of cot-side non-nutritive sucking assessment (suckometry) from the first postnatal days in very preterm infants; and (2) to characterise early sucking performances before and after routine implementation of a structured oral stimulation protocol.
Very preterm infants - born before 33 weeks gestational age - enrolled in a single-centre level III neonatal unit. Sucking performance measured weekly using a novel bedside suckometer from the first postnatal week until full oral feeding autonomy. Clinical outcomes and sucking parameters compared between non-stimulated (NOSTIM) and stimulated (STIM) groups.
연구 개요
상세 설명
The structured oral stimulation protocol was developed with reference to the Fucile protocol (Fucile et al., 2002) and the Premature Infant Oral Motor Intervention (PIOMI; Lessen et al., 2015). It involved gentle perioral stimulation using a gloved finger, progressing from the ear to the labial commissure. Responsive infants received escalating stimulation of the lips and intraoral structures (gums, palate, tongue). Sessions delivered 2-4 times daily by trained nurses during routine care, initiated within the first three postnatal days and continued until the introduction of oral feeding.
The suckometer (ICube Laboratory, UMR7357 Centre National Recherche Scientifique, Strasbourg) comprises a silicone teat connected to dual micro-pressure sensors quantifying suction (negative) and compression (positive) pressures in real time. Quantitative parameters include sucking peak frequency, compression peak frequency, and burst frequency.
연구 유형
등록 (실제)
연락처 및 위치
연구 장소
-
-
-
Lyon, 프랑스, 69004
- Neonatal Unit, Hopital Croix Rousse
-
-
참여기준
자격 기준
공부할 수 있는 나이
- 어린이
건강한 자원 봉사자를 받아들입니다
샘플링 방법
연구 인구
설명
Inclusion Criteria:
- Gestational age at birth: 27 to 32 weeks
- Admitted to the level III neonatal intensive care unit, Hôpital de la Croix-Rousse, Lyon
Exclusion Criteria:
- Ongoing sedation or analgesia
- Severe neurological injury: intraventricular haemorrhage grade ≥2 or periventricular leukomalacia
- Major congenital anomalies or chromosomal abnormalities
- Necrotising enterocolitis
공부 계획
연구는 어떻게 설계됩니까?
디자인 세부사항
코호트 및 개입
그룹/코호트 |
개입 / 치료 |
|---|---|
|
NOSTIM group
Infants hospitalised before the implantation of Structured Oral Stimulation Protocol
|
Bedside non-nutritive suckometer comprising a silicone teat connected to dual micro-pressure sensors.
Quantifies suction (negative) and compression (positive) pressures in real time.
Measurements performed weekly from the first postnatal week until full oral feeding autonomy in all participants.
|
|
STIM group
Infants hospitalised after the implantation of Structured Oral Stimulation Protocol
|
Bedside non-nutritive suckometer comprising a silicone teat connected to dual micro-pressure sensors.
Quantifies suction (negative) and compression (positive) pressures in real time.
Measurements performed weekly from the first postnatal week until full oral feeding autonomy in all participants.
The structured oral stimulation protocol was developed with reference to the Fucile protocol (Fucile et al., 2002) and the Premature Infant Oral Motor Intervention (PIOMI; Lessen et al., 2015).
It involved gentle perioral stimulation using a gloved finger, progressing from the ear to the labial commissure.
Responsive infants received escalating stimulation of the lips and intraoral structures (gums, palate, tongue).
Sessions delivered 2-4 times daily by trained nurses during routine care, initiated within the first three postnatal days and continued until the introduction of oral feeding.
|
연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Feasibility of bedside suckometry (successful recordings rate)
기간: From first postnatal week until full oral feeding autonomy, up to approximately 7 weeks
|
Proportion of infants with successful suckometry recordings from the first postnatal week.
Feasibility defined as absence of adverse events and completion of weekly assessments.
|
From first postnatal week until full oral feeding autonomy, up to approximately 7 weeks
|
2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Suction burst frequency
기간: Weekly from first postnatal week to full oral feeding autonomy, up to 7 weeks
|
Number of suction bursts per session compared between STIM and NOSTIM groups over time
|
Weekly from first postnatal week to full oral feeding autonomy, up to 7 weeks
|
공동 작업자 및 조사자
수사관
- 수석 연구원: jean-charles picaud, md, phd, Hopital croix rousse
간행물 및 유용한 링크
일반 간행물
- Lau C, Smith EO. A novel approach to assess oral feeding skills of preterm infants. Neonatology. 2011;100(1):64-70. doi: 10.1159/000321987. Epub 2011 Jan 5.
- Lau C. Development of infant oral feeding skills: what do we know? Am J Clin Nutr. 2016 Feb;103(2):616S-21S. doi: 10.3945/ajcn.115.109603. Epub 2016 Jan 20.
- Zhao S, Jiang H, Miao Y, Liu W, Li Y, Zhang Y, Wang A, Cui X. Effects of implementing non-nutritive sucking on oral feeding progression and outcomes in preterm infants: A systematic review and meta-analysis. PLoS One. 2024 Apr 16;19(4):e0302267. doi: 10.1371/journal.pone.0302267. eCollection 2024.
- Lessen BS, Morello CA, Williams LJ. Establishing Intervention Fidelity of an Oral Motor Intervention for Preterm Infants. Neonatal Netw. 2015;34(2):72-82. doi: 10.1891/0730-0832.34.2.72.
- Fucile S, Gisel E, Lau C. Oral stimulation accelerates the transition from tube to oral feeding in preterm infants. J Pediatr. 2002 Aug;141(2):230-6. doi: 10.1067/mpd.2002.125731.
연구 기록 날짜
연구 주요 날짜
연구 시작 (실제)
기본 완료 (실제)
연구 완료 (실제)
연구 등록 날짜
최초 제출
QC 기준을 충족하는 최초 제출
처음 게시됨 (실제)
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
QC 기준을 충족하는 마지막 업데이트 제출
마지막으로 확인됨
추가 정보
이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .