Assessing the Effectiveness of a Novel Contact Lens (Ortho C) on Paediatric Nearsightedness and Mood

Not Applicable

• Conditions: myopia; negative mood; Eye - Diseases / disorders of the eye; Mental Health - Studies of normal psychology, cognitive function and behaviour

• Registration Number: ACTRN12624000565549
• Lead Sponsor: niversity of Waterloo

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2024-05-05
• Last Update Posted: 13 May 2024

Recruitment & Eligibility

• Status: ot yet recruiting
• Sex: All
• Target Recruitment: 50

Inclusion Criteria

Include participants 6 to 16 years of age with myopia.

Exclusion Criteria

None.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Visual acuity[Snellen visual acuity chart A visual acuity test is conducted at the end of every week during the first 4 weeks and at the end of every second week for the next 3 weeks.]

Secondary Outcome Measures

Name	Time	Method
Mood[Mood Assessment Sheet, Greenberger and Padesky (2016) The participant’s Mood Assessment Sheet is reviewed at the end of every week during the first 4 follow-ups and at the end of every second week for the next 3 follow-ups. ];Self-Esteem[Hare Self-Esteem Scale Baseline and at the end of the follow-up periods (at the end of 10 weeks).];Quality of Life[Kidscreen Quality of Life Baseline and at the end of the follow-up periods (at the end of 10 weeks).]