Trial · NCT07903766
Effects of a Multisensory Intervention Program on the Term Behavior of the Very Premature Baby
NCT07903766, Not applicable, Not yet recruiting, Assistance Publique Hopitaux De Marseille
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Effects of a Multisensory Intervention Program on the Term Behavior of the Very Premature Baby. Trials, record NCT07903766. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07903766
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Effects of a Multisensory Intervention Program on the Term Behavior of the Very Premature Baby
- NCT number
- NCT07903766
- Status
- Not yet recruiting
- Phases
- Not applicable
- Enrollment
- 144 participants, estimated
- Lead sponsor
- Assistance Publique Hopitaux De Marseille
- Conditions
- Very Premature Baby
- Interventions
- Multisensory intervention program, Standard care
- First posted
- 2026-10-29
- Last updated
- 2026-10-29
Source ClinicalTrials.gov
Registered outcomes12
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Assessment of preterm behavior using the NICU Network Neurobehavioral Scale (NNNS) neurobehavioral scale | 37 weeks of amenorrhea before the premature baby is discharged from hospital | The NNNS neurobehavioral scale comprises 13 dimensions: habituation (3 items rated between 1 and 9), orientation (7 items rated between 1 and 9), self-regulation (15 items rated between 1 and 9), hypertonia (10 items rated between 0 and 10), hypotonia (10 items rated between 0 and 10), asymmetry reflexes (16 items rated between 0 and 16), non-optimal reflexes (15 items rated between 0 and 15), excitability (15 items rated between 0 and 15), lethargy (15 items rated between 0 and 15), arousal (7 items rated between 1 and 9), quality of movement (6 items rated between 1 and 9), stress ( 50 items rated between 0 and 1) and handling tolerance (8 items rated between 0 and 1). This assessment is carried out at 37 weeks of amenorrhea by a trained pyschomotrician before the premature baby is discharged from hospital Higher scores reflect better neurobehavioral construction. |
| Secondary | Average weight gain (g/kg/d) | Day -1, at Day 1 and Day 10, at discharge and at 3 months corrected age | |
| Secondary | Baby's tolerance of multi-sensory stimulation | days 1, 2, 3, 4, 5, 6, 7, 8, 9 and 10 of the multi-sensory stimulation | Simplified NIDCAP grid evaluation (Tolerance) |
| Secondary | Total length of hospital stay | At the time of hospital discharge (up to 6 months) | Number of days in hospital |
| Secondary | Duration of skin-to-skin contact per day from inclusion to incubator discharge | during hospitalisation (up to 6 months) and at the time of hospitalisation discharge (up to 6 months) | Hour(s)/day of skin-to-skin contact |
| Secondary | Duration of breast-feeding | At the time of hospital discharge (up to 6 months) and at the medical consultation at 3 months of corrected age | Number of days breastfeeding or bottle-feeding with breast milk |
| Secondary | Post-traumatic stress of mother and father | At the medical consultation at 3 months of corrected age | Parents will complete the Perinatal Posttraumatic stress disorder (PPQ) questionnaire |
| Secondary | Mother's and father's anxiety levels | At inclusion, at the baby's discharge from hospital (up to 6 months), and at the medical consultation at 3 months of corrected | Anxiety symptoms will be assessed using the Spielberger scale : from a score of 20 (no anxiety) to a score of 80 (high anxiety) |
| Secondary | Quality of life of mother and father | At the medical consultation at 3 months of corrected age | Quality of life will be assessed using the questionnaire (SF 36) |
| Secondary | Spontaneous motricity | At the medical consultation between 3 and 4 months of corrected age | Spontaneous motricity will be assessed using the Prechtl technique via video recording |
1 to 10 of 12Source ClinicalTrials.gov
See all 12 registered outcomesOutcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT07903766
GET https://conductscience.org/api/trials/v1/NCT07903766/registered