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Evaluation of the Efficacy of Optometric Rehabilitation on Visual Cognitive Deficits in Children

Evaluation of the Efficacy of Optometric Rehabilitation on Visual Cognitive Deficits in Children

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02061501
Enrollment
70
Registered
2014-02-12
Start date
2014-06-30
Completion date
2017-06-30
Last updated
2014-06-23

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

Conditions

Visual Cognitive Deficits

Keywords

visual cognitive deficits

Brief summary

Visual cognitive deficits in children are frequent, with an impact on working and daily activities. Optometric therapy may improve those functions, however few studies have been performed. We aim to evaluate the efficacy of such therapy by a comparative study between two groups of children aged between 5 and 12 after 6 months of rehabilitation.

Interventions

OTHEROptometric therapy during 6 months

Optometric therapy during 6 months, once a week

OTHEROptometric therapy during 12 months

Optometric therapy once a week, during 12 months

Sponsors

University Hospital, Strasbourg, France
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
5 Years to 12 Years
Healthy volunteers
No

Inclusion criteria

* visual cognitive deficits * normal intelligence

Exclusion criteria

* cerebral palsy * mental deficiency * visual acuity deficit

Design outcomes

Primary

MeasureTime frameDescription
Calculation of a composite score at Visit 1Visit 1 (6 months of rehabilitation)The composite score is calculated from the results obtained at several neuropsychology and optometric tests. Basal score is calculated at Visit 0 (inclusion visit).

Secondary

MeasureTime frameDescription
Calculation of a composite score at Visit 2Visit 2 (12 months of rehabilitation)The composite score is calculated from the results obtained at several neuropsychology and optometric tests.

Other

MeasureTime frameDescription
Quality of lifeVisit 2 (12 months of rehabilitation)Quality of life assessed by a questionnaire at V0, V1 and V2.

Countries

France

Contacts

Primary ContactAnne de Saint Martin, MD
anne.desaintmartin@chru-strasbourg.fr03 88 12 83 28

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026