Sensory Processing Skills in Toddler With Joint Hypermobility

Sponsor
Gazi University (Other)
Overall Status
Completed
CT.gov ID
NCT06041191
Collaborator
(none)
58
1
3
19.2

Study Details

Study Description

Brief Summary

shows that children and adults with joint hypermobility may be identified with common clinical problems that are unrelated, such as chronic fatigue, anxiety, and a range of gastrointestinal functional disorders [4-6]. Considering the relationship of joint hypermobility with joint muscle tone and posture, sensory processing skills may also be affected in individuals with hypermobility. No study in the literature examines the relationship between joint hypermobility and sensory processing. This study was planned to detect joint hypermobility as early as 12-14 months and to examine its relationship with sensory processing skills.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: Assessment

Study Design

Study Type:
Observational
Actual Enrollment :
58 participants
Observational Model:
Cohort
Time Perspective:
Cross-Sectional
Official Title:
An Investigation of Sensory Processing Skills in Toddler With Joint Hypermobility
Actual Study Start Date :
Jun 1, 2023
Actual Primary Completion Date :
Jul 15, 2023
Actual Study Completion Date :
Sep 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Children with GJH

Children who scored above 4 points in the hypermobility assessment made with the Beighton score were included in this group. sensory processing skills assessed with the Test of Sensory Functions in Infants

Diagnostic Test: Assessment
The children included in the study were evaluated in terms of hypermobility and then divided into two groups. Children in both groups were evaluated in terms of sensory processing skills.

Children without GJH

Children who scored below 4 points in the hypermobility assessment made with the Beighton score were included in this group. sensory processing skills assessed with the Test of Sensory Functions in Infants

Diagnostic Test: Assessment
The children included in the study were evaluated in terms of hypermobility and then divided into two groups. Children in both groups were evaluated in terms of sensory processing skills.

Outcome Measures

Primary Outcome Measures

  1. Beighton Score [20minutes]

    . The test consists of 5 items: (1) positive if the passive dorsiflexion of the fifth metacarpophalangeal joint score is greater than 90 degrees (bilateral test); (2) positive if passive hyperextension of the elbow joint is >10 (bilateral test); (3) positive if passive hyperextension of the knee joint is >10 (bilateral test); (4) passive apposition of the thumb to the flexor side of the forearm is positive for joint hypermobility (bilateral test) if the shoulder is at 90 flexion, the elbow is extended, and the whole thumb is touching the flexor side of the forearm; and (5) the score is positive when dorsiflexion of the ankle is >30 (bilateral test). The assessment was performed on both the right and left sides, and the item was given 1 point if hypermobility was detected in the joints, and 0 points if not, according to the instructions of each item. Cut-off score of >4 was used to define hypermobility

Secondary Outcome Measures

  1. Test of Sensory Functions in Infants [20 minutes]

    The TSFI is primarily used to assess sensory defense behaviors in infants aged 4-18 months. Test; It consists of 5 subsections and 24 items. TSFI requires the infant to be stimulated and interact with a variety of materials. The total score varies between 0-49 and the test has norm values for different age groups. Although it is used from the fourth month, the most reliable and valid results are obtained between 7-18 months.

Eligibility Criteria

Criteria

Ages Eligible for Study:
12 Months to 14 Months
Sexes Eligible for Study:
All
Inclusion Criteria:

12-14 month old healthy children

-

Exclusion Criteria:
  • they had major congenital malformations, had genetic or chromosomal abnormalities, had known metabolic disorders, or had seizures.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Erzurum Technical University Erzurum Turkey

Sponsors and Collaborators

  • Gazi University

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Ayse Simsek, assistant professor, Gazi University
ClinicalTrials.gov Identifier:
NCT06041191
Other Study ID Numbers:
  • E-77082166-604.01.02-687785
First Posted:
Sep 18, 2023
Last Update Posted:
Sep 18, 2023
Last Verified:
Sep 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 18, 2023