Effects of video presented information about Excimer laser therapy on comprehension and satisfaction with informed consent

Not Applicable

Completed

• Conditions: Excimer laser treatment for ametropia; Eye Diseases

• Registration Number: ISRCTN54821973
• Lead Sponsor: Augenklinik Luzerner Kantonsspital [Cantonal Hospital Lucerne Eye Clinic]

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2017-05-10
• Study Completion: 2019-01-01
• Last Update Posted: 21 January 2020

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 86

Inclusion Criteria

1. Patients assessing refractive excimer laser therapy for ametropia at the refractive centre of the LUKS will be evaluated at their initial visit for study inclusion
2. Signed written informed consent form

Exclusion Criteria

1. Inability to follow the procedures of the study due to i.e. language problems, psychological disorders, dementia etc
2. Aged < 18 years
3. Enrolment of the investigator, his/her family members, employees and other dependent persons

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Patients knowledge is measured using five multiple choice questions with five statements after the consultation.

Secondary Outcome Measures

Name	Time	Method
<br> 1. Patients’ satisfaction is measured using a questionnaire after the consultation.<br> 2. Anxiety levels is measured using a subpart of the State-Trait Anxiety Inventory 42 after the consultation.<br> 3. Perceived contact time measured using a questionnaire after the consultation.<br>