Post-operative Satisfaction With Glaucoma Surgery Trial

This study is ongoing, but not recruiting participants.
Sponsor:
Information provided by (Responsible Party):
Congdon Nathan, Sun Yat-sen University
ClinicalTrials.gov Identifier:
NCT01726569
First received: November 10, 2012
Last updated: April 10, 2013
Last verified: April 2013

November 10, 2012
April 10, 2013
December 2012
December 2013   (final data collection date for primary outcome measure)
postoperative satisfaction rate in both group [ Time Frame: after surgery up to 6 weeks ] [ Designated as safety issue: No ]
the rate of satisfaction
Same as current
Complete list of historical versions of study NCT01726569 on ClinicalTrials.gov Archive Site
  • knowledge about glaucoma [ Time Frame: before surgery and after surgey 1 week and 6 weeks ] [ Designated as safety issue: No ]
    the knowledge about glaucoma scores
  • willingness to recommend surgery [ Time Frame: after surgery 1 week and 6 weeks ] [ Designated as safety issue: No ]
    The rate of willingness to recommend surgery
  • personality in both groups [ Time Frame: Baseline (before surgery) ] [ Designated as safety issue: No ]
    use Eysenck Personality Questionnaire-Revised Short Scale for Chinese(EPQ_RSC) access glaucoma patients personality
  • intraocular pressure and visual acuity in both groups [ Time Frame: before surgery and after surgery 1week and 6 weeks ] [ Designated as safety issue: No ]
    intraocular pressure and visual acuity in both groups
Same as current
Not Provided
Not Provided
 
Post-operative Satisfaction With Glaucoma Surgery Trial
A Randomized Trial of the Impact of Multifaceted Education on Post-operative Satisfaction With Glaucoma Surgery in Rural China
  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.

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.

Interventional
Not Provided
Allocation: Randomized
Endpoint Classification: Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Supportive Care
Glaucoma
  • 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.
  • Experimental: 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 and follow up counseling after operation 1 week and 6 weeks
    Interventions:
    • Behavioral: film and trained counseling
    • Other: traditional counseling
  • traditional counseling
    Subjects will be participate or not participate in pre-operative counseling and/or post-operative counseling with a rural hospital's doctor/nurse.
    Intervention: Other: traditional counseling
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Active, not recruiting
356
March 2014
December 2013   (final data collection date for primary outcome measure)

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
Both
18 Years and older
No
Contact information is only displayed when the study is recruiting subjects
China
 
NCT01726569
ZOC-CREST1
Yes
Congdon Nathan, Sun Yat-sen University
Sun Yat-sen University
Not Provided
Principal Investigator: Nathan Congdon, MD,MPH Zhongshan Ophthalmic Center,Sun Yat-sen University;ORBIS
Sun Yat-sen University
April 2013

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP