Post-operative Satisfaction With Glaucoma Surgery Trial

Glaucoma Clinical Trial

Official title:

A Randomized Trial of the Impact of Multifaceted Education on Post-operative Satisfaction With Glaucoma Surgery in Rural China

Clinical Trial Details — Status: Withdrawn

Administrative data

• NCT number: NCT01726569
• Other study ID #: ZOC-CREST1
• Status: Withdrawn
• Phase: N/A
• Start date: December 2012
• Est. completion date: March 2014

Study information

• Verified date: December 2021
• Source: Sun Yat-sen University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

1. Investigate degree of postoperative satisfaction in county level hospital glaucoma patients.

2. Investigate the effect of educational intervention affect the degree of satisfaction in glaucoma patients.

3. Investigate the effect factors of postoperative satisfaction.

Description:

Glaucoma is the leading cause irreversible blindness worldwide, but only less than 10% glaucoma patients were diagnosed in the country of Asia areas. In the country of China, patients who are low educational level and less known acknowledgement and information have less known glaucoma. In the help of the government and some international non-governmental organizations(NGOs), a lot of people in the country know the cataract, and the operability of cataract is increase. Because vision loss usually development after operation for glaucoma. If patients did not understand this, they may be not only do not accept operation, but also affect operability of cataract. We hope the educational intervention for glaucoma can increase the degree of satisfaction in glaucoma patients.

Recruitment information / eligibility

• Status: Withdrawn
• Enrollment: 0
• Est. completion date: March 2014
• Est. primary completion date: December 2013
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• age=18 years, glaucoma patients who do the peripheral iridectomy or trabeculotomy

Exclusion Criteria:

• patients who had been the trabeculotomy, vision=0.05, severe psychotic disorders and dysgnosia

Related Conditions & MeSH terms

• Glaucoma

Intervention

Behavioral:
• film and trained counseling
Subjects will be asked to watch a 5-10 min film and participate in a 10-15 min pre-operative counseling session with a trained doctor/nurse. Subjects will also participate in a 5 min post-operative counseling session.

Other:
• traditional counseling
Subjects will be not participate or participate in a pre-operative/post-operative counseling session with a rural hospital's doctor/nurse as usual traditional methods.

Locations

Country	Name	City	State
China	Sun Yat-sen University	Guangzhou	Guangdong

Sponsors (1)

Lead Sponsor	Collaborator
Sun Yat-sen University

Country where clinical trial is conducted

China, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	postoperative satisfaction rate in both group	the rate of satisfaction	after surgery up to 6 weeks
Secondary	knowledge about glaucoma	the knowledge about glaucoma scores	before surgery and after surgey 1 week and 6 weeks
Secondary	willingness to recommend surgery	The rate of willingness to recommend surgery	after surgery 1 week and 6 weeks
Secondary	personality in both groups	use Eysenck Personality Questionnaire-Revised Short Scale for Chinese(EPQ_RSC) access glaucoma patients personality	Baseline (before surgery)
Secondary	intraocular pressure and visual acuity in both groups	intraocular pressure and visual acuity in both groups	before surgery and after surgery 1week and 6 weeks