CClinicalTrials.gg
Enrolling by invitationNCT06608576BBL-ATOPUpdated Sep 23, 2024

Telematic Support in Early Intervention on Infants At Risk of Neurodevelopmental Delays

An interventional study of Face-to-face standard treatment and Telematic Support in High-risk Infants, sponsored by Universidad de Granada. Enrolling by invitation at 1 site in Spain. Open to participants aged 3 Months to 12 Months. Per ClinicalTrials.gov, last updated 2024-09-23.

Sponsored by Universidad de Granada · Not applicable, Interventional, and Supportive care

From the registry’s dates

  • Primary completion was expected by Jul 2025, 1 year 2 months ago, but the record still lists the study as enrolling by invitation.
  • Registered 7 months after the study started (first participant enrolled Feb 2024, registered Sep 2024).
Phase
Not applicable
Study type
Interventional
Enrollment
60
Allocation
Randomized
Ages
3 Months to 12 Months
Sex
All
01

Study summary

The purpose of this study is to evaluate the effects of early intervention support sessions via video conferencing as an adjuvant option to motor development on infants at risk of neurodevelopmental delays or disorders.

Read the detailed description

The parents will be informed about the procedure and will be given a written informed consent in order to participate in the study. Then, the families will be randomized into one of two groups: standard treatment or telematic support. Both treatments in a 2-month period.

02

Conditions studied

  • High-risk Infants

Keywords

  • early intervention
  • telerehabilitation
  • physical therapy
  • child development
03

In context

Lead sponsor

Universidad de Granada is the lead sponsor of 241 studies on the registry; 41 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
3 Months to 12 Months
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Minor infants with a chronological or corrected age of 3 to 12 months and their parents attending physical therapy early intervention protocol at the Neuropediatrics and Neurodevelopment Unit of San Cecilio University Hospital in Granada.
  • At risk of neurodevelopmental delays or disorders.
  • Whose family has a cell phone with WhatsApp Application installed and internet to be able to carry out the telematic tests.

Exclusion criteria

Exclusion Criteria:

  • Independent walking children.
  • Minor infants with diagnosis of neuromotor injury, visual and auditory sensory disorders or congenital anomalies.
  • Infants with orthoses and/or prostheses.
  • Children with health complications that enable the child's participation in the study.
  • Not spanish-speaking parents.
05

Study design

Phase
Not applicable
Primary purpose
Supportive care
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
60 participants (estimated)

Study arms

  • Active comparator
    Standard Treatment

    participants will receive face-to-face early intervention treatment on physical therapy area once a month for two months.

    Other: Face-to-face standard treatment

  • Experimental
    Telematic Support

    Participants will receive weekly telematic early intervention sessions at home via video conferencing for two months.

    Other: Telematic Support

Interventions

  • OtherFace-to-face standard treatment

    Individualized early intervention treatment on physical therapy area as usual in the early intervention facilities once a month for two months. Instructions will be given to the parents for follow-up at home to stimulate the baby's motor development until next face-to-face session.

  • OtherTelematic Support

    The physiotherapist in charge of the telematic sessions will review and guide in real time through WhatsApp platform, the performance and active participation of the parents in the therapeutic activities being asked to follow-up at home in the face-to-face appointment, correcting, as necessary.

06

What researchers measure

Primary outcomes

  1. Change from Baseline in Motor Development on the Motor scale of the Infant Motor Development on the Bayley Scales of Infant and Toddler Development-III® (BSID-III) at month 2.

    The BSID-III is an assessment tool for diagnosing developmental delays in early childhood from 1 to 42 months. It assesses 5 developmental domains: Cognitive Scale, Language Scale, Motor scale, Social-Emotional Scale and Adaptative Scale. The motor scale has 66 items in the fine motor and 72 items in the gross motor domain which are administrated according to the child development. Change= (2 months development score - baseline Score).

    Time frame: Baseline and Month 2.

  2. Change from Baseline in maturation of motor skills on the Alberta Infant Motor Scale (AIMS) at month 2.

    The AIMS is an observational assessment tool that requires minimal handling of an infant by the examiner. It assesses the maturation of infant's motor skills from term (40 weeks gestation) to 18 months. It has 58 observational items divided into four subscales which are prone, supine, sitting and standing. Change= (2 months development score - baseline Score).

    Time frame: Baseline and Month 2.

  3. Change from Baseline in infant motor behaviour and motor development on the Infant Motor Profile (IMP) at month 2.

    The IMP is a video-based assessment for infants aged 3 to 18 months. It assesses the spontaneous motor behaviour in supine, prone, sitting, standing, walking and during reaching and grasping - depending on the age of the infant. Includes 5 domains: the size of the infant's motor repertoire, the infant's ability to make an adaptive selection out of his/her repertoire, performance, symmetry and fluency. Change= (2 months IMP total and subscales scores - baseline scores).

    Time frame: Baseline and Month 2.

Secondary outcomes

  1. Change from Baseline in parents' quality of life on the Care-related quality of life (CarerQol) at month 2.

    CarerQol measures the impact of providing informal care on caregivers. Consists of seven items questionnaire to evaluate the impact of informal care on satisfaction, support, problems with daily activities, and financial, relational, mental health and physical health problems of caregivers, and a Visual Analogue Scale which measures general well-being in terms of happiness from 0 (completely unhappy) to 10 (completely happy). Change= (2 months scores on each item - baseline Score).

    Time frame: Baseline and Month 2.

  2. Change from Baseline in levels of stress experienced by parents on the Parental Stress Scale (PSS) at month 2.

    The Paretal Stress Scale is an 18-item self-report measure design to assess the perceived levels of stress resulting from being a parent. Overall possible scores on the scale range from 18 to 90 with higher scores indicating a higher level of stress. There are no average scores or "cut-off's" for this tool. Change= (2 months stress score - baseline score).

    Time frame: Baseline and Month 2.

  3. Parents satisfaction with the telematic support service measured with the Client Satisfaction Questionnaire (CSQ-8).

    The Client Satisfaction Questionnaire is an 8-item measure of client or consumer satisfaction with health and human services including governmental and public benefit programs and services. Overall possible scores on the scale range from 8 to 32 with higher scores indicating a higher level of satisfaction with the given service. There are no average scores or "cut-off's" for this tool.

    Time frame: Month 2

  4. Change from Baseline in parental self-efficacy and satisfaction of being a parent on the Parenting Sense of Competence (PSOC) at month 2.

    PSOC is a self-report measure that uses 17 questions to measure how capable a caregiver feels as a parent and how satisfied they are with being a parent. Possible scores range from 17 to 102 with higher scores indicating a higher parenting sense of competency. There are no average scores or "cut-off's" for this tool. Change= (2 months sense of competence score - baseline score).

    Time frame: Baseline and Month 2.

07

Study locations

1 site
  • Hospital Universitario San Cecilio de Granada
    Granada, 18007, Spain
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 23, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT06608576
Lead sponsor
Universidad de Granada
Collaborators
Hospital Universitario San Cecilio de Granada
Responsible party
Marie Carmen Valenza (PT, PhD, Professor at University of Granada, Universidad de Granada) — Principal investigator
First posted
Sep 23, 2024
Start date
Feb 15, 2024
Primary completion
Jul 31, 2025 (estimated)
Completion
Jul 31, 2025 (estimated)
Last update
Sep 23, 2024

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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