Feeding Difficulties

6

Review clinical trials related to Feeding Difficulties. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Premature Infant Oral Motor Intervention vs. Pacifier for Oral Feeding Transition in Preterm Infants

This study compares three approaches to help premature babies learn to feed by mouth: a special mouth exercise program (called PIOMI), using a pacifier, and standard care. Premature babies often have difficulty feeding because their sucking, swallowing, and breathing are not yet coordinated, which can lead to longer hospital stays. The study will include 150 premature infants born between 26 and 32 weeks of pregnancy at a hospital in Thi Qar. Babies will be randomly placed into one of three groups: one group will receive a many-day mouth exercise program, another will use a pacifier for many days, and the third will receive routine care. We will measure how quickly each baby learns to feed fully by mouth, how long they stay in the hospital, how much weight they gain, and their feeding skills. The results may help improve care for premature babies and reduce the time they spend in the hospital.

Participants needed: 150
Trial details
Age: 1-28Biological sex: AllType: InterventionalSponsor: University of BaghdadUpdated: Mar 10, 2026Locations: 1
Eligibility criteria

- Preterm infants born at 26-32 weeks of gestational age [+3]

Orofacial malformations (e.g., cleft lip, cleft palate) [+5]

Status: Recruiting

Feeding Difficulties and Quality of Life in Children With Tracheal Cannula

The over all goal of this observational study is to study if there is an association between the presence of feeding difficulties and self-assessed quality of life in children with tracheal cannula. The main questions it aims to answer are 1. What is the incidence of feeding difficulties in children with tracheostomy and what type of feeding difficulties affect these children? 2. How do children with a tracheal tube and their parents assess their quality of life measured through PedsQL? 3. Is there an association between the presence of feeding difficulties and self-assessed quality of life in children with tracheal cannula? Quality of life will be assessed in an interview using the PedsQL instrument generic module 4.0. Swallowing difficulties will be assessed through evaluations based on The Montreal Children's Hospital Feeding Scale.

Participants needed: 80
Trial details
Age: Up to 18Biological sex: AllType: ObservationalSponsor: Karolinska InstitutetUpdated: Feb 13, 2026Locations: 2
Eligibility criteria

Not listed

Status: Not yet recruiting

The Use of High Bile-binding Foods to Reduce Upper Gastrointestinal Bile Acid Concentrations (Aim 2)

Using a four-week randomized, crossover study design, we will assess the impact of 2 weeks of a high bile acid-binding blenderized diet, compared to 2 weeks of a low bile acid-binding blenderized diet, on gastric and salivary bile acid concentrations within individual participants. Four weeks of an amino acid formula will be a comparator group.

Participants needed: 66
Trial details
Phase: Phase 4Age: 5-21Biological sex: AllType: InterventionalSponsor: Boston Children's HospitalUpdated: Dec 26, 2025
Eligibility criteria

receive blenderized feeds or will start receiving blenderized feeds [+3]

have undergone anti-reflux surgery [+10]

Status: Recruiting

The Use of High Bile-binding Foods to Reduce Upper Gastrointestinal Bile Acid Concentrations (Aim 1)

We will perform an acute physiology study comparing three different diets-an amino acid-based formula, a low bile acid-binding blenderized diet, or a high bile acid-binding blenderized diet administered through gastrostomy tube. We will determine the differences in gastric and salivary bile acid concentrations between participants over the 4 hour post-prandial timeframe. Participants who regularly receive an amino acid-based formula will receive an amino acid-based formula during the study and participants who regularly receive a blenderized feed will receive a blenderized feed during the study. Only participants who regularly receive blenderized feeds will be randomized to receive either the high or low bile acid binding blenderized feed.

Participants needed: 60
Trial details
Phase: Phase 4Age: 5-21Biological sex: AllType: InterventionalSponsor: Boston Children's HospitalUpdated: Dec 26, 2025Locations: 1
Eligibility criteria

receive at least 80% of their nutritional needs by gastrostomy [+2]

have received a fundoplication [+3]

Status: Not yet recruiting

The Use of High Bile-Binding Foods to Reduce Upper Gastrointestinal Bile Acid Concentrations (Aim 3)

Using a longitudinal cohort design, we will compare the impact of a high BA-binding blenderized diet compared to a low BA-binding blenderized diet and an amino acid-based formula, on gastrointestinal and pulmonary hospitalization and emergency room visit rates over six months.

Participants needed: 138
Trial details
Age: 5-21Biological sex: AllType: ObservationalSponsor: Boston Children's HospitalUpdated: Dec 30, 2025
Eligibility criteria

receive at least 80% of their nutritional needs via gastrostomy [+2]

have undergone anti-reflux surger [+2]

Status: Recruiting

Stereotypic Behaviors and Feeding Difficulties in Adults With Developmental Disabilities

Adults with developmental disabilities (DD) and autism represent a vulnerable demographic that transitions into adulthood with diverse etiologies, exhibiting a significantly higher prevalence of various challenging behaviors. These problematic behaviors can lead to adverse health outcomes and a diminished quality of life. Addressing these issues often necessitates an interdisciplinary approach to continuity of care, focusing on enhancing functional skills, empowerment, and independence, as well as preventing and mitigating challenging behaviors. The current research proposal comprises of three studies designed to evaluate the efficacy of behavioral interventions for problematic behaviors in adults with DD and autism. If left unaddressed, these behaviors may worsen over time, potentially hindering community involvement, educational opportunities, and employment prospects. These include harmful stereotypies and feeding difficulties.

Participants needed: 8
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Oslo University HospitalUpdated: Apr 15, 2025Locations: 1
Eligibility criteria

Participants will be recruited through referrals at the Department of Neurohabil... [+3]

If there are medical causes of the participant's behavioral problem or [+6]