Improvement in Preschoolers' Participation as a Result of Occupational Therapy Intervention
NCT ID: NCT02774135
Last Updated: 2021-04-21
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
52 participants
OBSERVATIONAL
2017-05-01
2021-04-19
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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direct occupational therapy intervention
group will be evaluated 4 times: on referral to waiting list for treatment, before and after 9-12 direct individual treatments of 45 minutes, and follow-up after 3 months.
direct occupational therapy intervention
Short term direct individual occupational therapy (9-12 weeks).Participants will receive occupational therapy intervention according to health law. The study will document the therapeutic intervention implemented in practice using the Documentation of Occupational Therapy Session during Intervention (DOTSI).
Interventions
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direct occupational therapy intervention
Short term direct individual occupational therapy (9-12 weeks).Participants will receive occupational therapy intervention according to health law. The study will document the therapeutic intervention implemented in practice using the Documentation of Occupational Therapy Session during Intervention (DOTSI).
Eligibility Criteria
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Inclusion Criteria
* Hebrew speaking
Exclusion Criteria
* Attending physiotherapy or psychology treatments
* Autistic Spectrum Disorder
* Cerebral Palsy
* Spina Bifida
* Developmental Intellectual Disabilities
* Blindness
* Deafness
54 Months
83 Months
ALL
Yes
Sponsors
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Tel Aviv University
OTHER
Clalit Health Services
OTHER
Responsible Party
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Dr. Gary Leonard Robinson
Dr, MD, Pediatrics
Principal Investigators
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Leonard G Robinson, Md
Role: PRINCIPAL_INVESTIGATOR
Clalit Health Services
Locations
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Clalit Health Services
Tel Aviv, , Israel
Countries
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Other Identifiers
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COM150203CTIL
Identifier Type: -
Identifier Source: org_study_id
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