Post-operative Satisfaction With Glaucoma Surgery Trial

NCT01726569 | Withdrawn DMC

• 1 other identifier: ZOC-CREST1
• Study Type: interventional
• Target: N/A
• Locations: 1 country
• Sites: 1

Brief Summary

1. 1.Investigate degree of postoperative satisfaction in county level hospital glaucoma patients.
2. 2.Investigate the effect of educational intervention affect the degree of satisfaction in glaucoma patients.
3. 3.Investigate the effect factors of postoperative satisfaction.

Conditions

Glaucoma

Keywords

glaucoma; educational intervention; post-operative satisfaction; knowledges

Outcome Measures

Primary Outcomes (1)

• postoperative satisfaction rate in both group

  the rate of satisfaction

  after surgery up to 6 weeks

Secondary Outcomes (4)

• knowledge about glaucoma

  before surgery and after surgey 1 week and 6 weeks

• willingness to recommend surgery

  after surgery 1 week and 6 weeks

• personality in both groups

  Baseline (before surgery)

• intraocular pressure and visual acuity in both groups

  before surgery and after surgery 1week and 6 weeks

Study Arms (2)

film and trained counseling

EXPERIMENTAL

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 and follow up counseling after operation 1 week and 6 weeks

Behavioral: film and trained counseling; Other: traditional counseling

traditional counseling

OTHER

Subjects will be participate or not participate in pre-operative counseling and/or post-operative counseling with a rural hospital's doctor/nurse.

Other: traditional counseling

Interventions

film and trained counseling BEHAVIORAL

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.

film and trained counseling

traditional counseling OTHER

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.

film and trained counseling; traditional counseling

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

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

You may not qualify if:

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

Sponsors & Collaborators

• Sun Yat-sen University: lead

Study Sites (1)

Sun Yat-sen University

Guangzhou, Guangdong, China

Location

MeSH Terms

Conditions

Glaucoma

Interventions

Motion Pictures

Condition Hierarchy (Ancestors)

Ocular Hypertension; Eye Diseases

Intervention Hierarchy (Ancestors)

Audiovisual Aids; Educational Technology; Technology; Technology, Industry, and Agriculture

Study Officials

• Nathan Congdon, MD,MPH

  Zhongshan Ophthalmic Center,Sun Yat-sen University;ORBIS

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: NONE
• Purpose: SUPPORTIVE CARE
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: Guangdong Educational Intervention for Rural Glaucoma surgical patient

Study Record Dates

• First Submitted: November 10, 2012
• First Posted: November 15, 2012
• Study Start: December 1, 2012
• Primary Completion: December 1, 2013
• Study Completion: March 1, 2014
• Last Updated: December 21, 2021

Record last verified: 2021-12

Locations

CN (1)