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Belly time in the development of premature newborns

Tummy time intervention in the neuromotor development of preterm newborns - randomized clinical trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-2nwkr47
Enrollment
Unknown
Registered
2022-02-15
Start date
2021-07-30
Completion date
Unknown
Last updated
2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Premature, Low Birth Weight, Motor Skills Disorders, Early Intervention

Interventions

Control Group: 20 Participants in the control group will receive guidance routinely offered by the care team of the follow-up clinic, physicians, nurses, physiotherapists, etc. Experimental group: The
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Sponsors

Departamento de Fisioterapia da Universidade Federal do Rio Grande do Norte
Lead Sponsor
Departamento de Fisioterapia da Universidade Federal do Rio Grande do Norte
Collaborator

Eligibility

Age
No minimum to 4 Months

Inclusion criteria

Inclusion criteria: Participants will be selected according to the following criteria: (1) neonates born between 30 wk and 36 wk and 6 days, according to ultrasound; (2) adequate for gestational age; (3) Apgar = 7 in the 5th minute; (4) birth weight less than 2500 g; (5) intrauterine growth restriction (6) absence of cardiorespiratory complications such as bronchopulmonary dysplasia and congenital heart diseases, neurological such as brain malformation, microcephaly, hydrocephalus, musculoskeletal disorders such as congenital clubfoot and congenital muscular torticollis, or auditory according to the little ear test; genetic syndromes, congenital infections (toxoplasmosis, syphilis, rubella, cytomegalovirus and herpes simplex) and visual changes according to the little eye test; (7) present poor or normal motor repertoire in the assessment of Generalized Movements (MG).

Exclusion criteria

Exclusion criteria: The following will be excluded: (1) babies diagnosed with grade III and IV intraventricular hemorrhage; (2) babies whose parents withdraw from participating (3) babies who do not attend 2 assessments to monitor primary and secondary outcomes, (4) parents do not answer the phone for 3 consecutive days to reschedule assessments or declare withdrawal from the intervention by of the guardians, (5) parents who do not fill out the field diary to monitor the practice of Tummy Time. After randomization, participants will be excluded if they present any health deterioration and need to be hospitalized, change state and/or country.

Design outcomes

Primary

MeasureTime frame
Improved head control motor performance, assessed by Kinovea® software

Secondary

MeasureTime frame
Improved development of gross motor function, assessed by the Bayley Scale of Child Development – ??III;Little or no change in vertical alignment and horizontal leveling of the head assessed by Kinovea® software

Countries

Brazil

Contacts

Public ContactSilvana Pereira

Universidade Federal do Rio Grande do Norte

silvana.alves@ufrn.br+55-084-991818144

Outcome results

None listed

Source: REBEC (via WHO ICTRP) · Data processed: Feb 10, 2026