Is There Any Correlation Among Neonates Anthropometry and Neuromotor Behaviour

NCT ID: NCT05361213

Last Updated: 2022-05-04

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Total Enrollment

54 participants

Study Classification

OBSERVATIONAL

Study Start Date

2021-08-12

Study Completion Date

2022-03-15

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

To explore the association among anthropometric parameters and neuromotor behaviour in neonates for early identification and prediction of later neuromotor deficit.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

The association between anthropometric (birth weight, length and occipitofrontal circumference) measurement and hands-on measurement of above mentioned anthropometric dimensions and demographic dimension (bilateral forearm, midarm, calf and thigh) with neuromotor behaviour were explored.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Cerebral Palsy, Autism or Other Neuromotor Behavior Abnormalities Correlation With Anthropometry

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

OTHER

Study Time Perspective

CROSS_SECTIONAL

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Neonates born between ≥28 weeks and ≤ 42 weeks of gestation
* Birth weight between 1500 and 3000 grams
* Neonates are born under all the classifications of Fenton growth charts (SGA, AGA and LGA)
* Stable Hemodynamics
* Free from infection
* Stable vitals

Exclusion Criteria

* Dermal conditions
* Chromosomal abnormalities
* History of surgery
* Neural tube defect
* Cardiac abnormally
Minimum Eligible Age

28 Weeks

Maximum Eligible Age

42 Weeks

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Asir John Samuel

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Asir John Samuel

Professor, Maharishi Markandeshwar Institute of physiotherapy and rehabilitation

Responsibility Role SPONSOR_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Asir John Samuel, PhD

Role: STUDY_DIRECTOR

Maharshi Markandeshwar institute of physiotherapy and rehabilitation, mullana, ambala, india

Sunanda Bhowmik, MPT

Role: STUDY_CHAIR

Maharshi Markandeshwar institute of physiotherapy and rehabilitation, mullana, ambala, india

Jaishree Rai, (MPT)

Role: PRINCIPAL_INVESTIGATOR

Maharshi Markandeshwar institute of physiotherapy and rehabilitation, mullana, ambala, india

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Jaishree

Ambāla, Haryana, India

Site Status

Countries

Review the countries where the study has at least one active or historical site.

India

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

MMDU/IEC/1924

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

The Alkmaar MLPTI Cohort Study: Outcomes at 9 Years
NCT05990582 ENROLLING_BY_INVITATION NA