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The pilot study for the effect of extra body weight application on pediatric patients with movement disorder

The pilot study for the effect of extra body weight application on pediatric patients with movement disorder

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
TCTR
Registry ID
TCTR20200224002
Enrollment
10
Registered
2020-02-24
Start date
2019-12-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Abnormal movement Abnormal movement weighted vest Sensory integration

Interventions

During data collection&#44
participants wore an invented jacket with weight or without weight. Participants were seated on a chair with full back support and feet touched the floor&#44
hip and knee flexed 90 degrees. The buttocks and thighs contacted with the chair. The box of toys with same shape and size 4x4 cm. was placed beside the participant. The cylindrical tube for dropping
1 meter high. Participants wore the jacket during doing the activity. After completing the first 20 toys&#44
there is 10 minutes break to change the weight of the jacket and then manipulate in the same activity. The video recorder was located on the side of the participant to record while doing the task. Ti
participants wearing the invented jacket without weight (2) The experimental condition&#44
applying weight 10% of body weight at trunk and arm
9% of body weight at trunk and 1% of body weight at arm The sequence of the weight was random. The weight was applied by another interventionist before the participant walked in the intervention room
pocketed denim long s
Experimental Device
Intervention

Sponsors

none
Lead Sponsor
none,none
Collaborator

Eligibility

Sex/Gender
All
Age
3 Years to 16 Years

Inclusion criteria

Inclusion criteria: - Age 3-16 Years old - Have medical record of movement disorder - Cooperative

Exclusion criteria

Exclusion criteria: - History of infection within 1 week before the study - Spastic of upper extremity MAS >2 - Have musculoskeletal complications interfering task-activity

Design outcomes

Primary

MeasureTime frame
Time of complete activity Immediately Time recording

Secondary

MeasureTime frame
Quality of upper extremity function Immediately Observe the video

Countries

Thailand

Contacts

Public ContactSavarose Sangchayosawat

Rehabilitation Medicine Department, Faculty of Medicine Siriraj Hospital, Mahidol University

mo.sangchayosawat@gmail.com0865137774

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 9, 2026