Uveitis in Relation to Perceived Stress: A Prospective Study

The recruitment status of this study is unknown because the information has not been verified recently.
Verified December 2009 by The New York Eye & Ear Infirmary.
Recruitment status was  Recruiting
Sponsor:
Information provided by:
The New York Eye & Ear Infirmary
ClinicalTrials.gov Identifier:
NCT01025986
First received: December 3, 2009
Last updated: NA
Last verified: December 2009
History: No changes posted
  Purpose

The purpose of this study is to conduct a prospective analysis to determine the relationship between disease activity of noninfectious uveitis and stress.


Condition
Uveitis

Study Type: Observational
Study Design: Observational Model: Cohort
Time Perspective: Prospective
Official Title: Uveitis in Relation to Perceived Stress: A Prospective Study

Resource links provided by NLM:


Further study details as provided by The New York Eye & Ear Infirmary:

Estimated Enrollment: 200
Study Start Date: July 2009
Groups/Cohorts
Noninfectious Uveitis

Detailed Description:

Patients presenting at The New York Eye and Ear Infirmary (NYEEI) who meet the inclusion criteria will be recruited prospectively. Patients diagnosed with non-infectious uveitis will be asked to self-administer the Perceived Stress Scale (PSS) - 10, following informed consent. Patient demographics will also be collected. The presence of inflammation will be then be assessed by the investigator. Patients will be asked to complete the PSS-10 again at all subsequent standard-of-care visits within a 6-month timeframe. PSS-10 scores are obtained by reversing the scores on the four positive items (4, 5, 7 and 8), then summing across all 10 items. Patient and the investigator will be masked to the PSS scores.

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Sampling Method:   Non-Probability Sample
Study Population

Patients presenting at the New York Eye and Ear Infirmary diagnosed with uveitis

Criteria

Inclusion Criteria:

  • At least 18 years of age with a diagnosis of non-infectious uveitis
  • Able to self-administer the Perceived Stress Scale (PSS) - 10

Exclusion Criteria:

  • Diagnosis of infectious uveitis
  Contacts and Locations
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the Contacts provided below. For general information, see Learn About Clinical Studies.

Please refer to this study by its ClinicalTrials.gov identifier: NCT01025986

Locations
United States, New York
The New York Eye and Ear Infirmary Recruiting
New York, New York, United States, 10003
Contact: Katy Tai, CCRC       ktai@nyee.edu   
Principal Investigator: C. Michael Samson, MD         
Sub-Investigator: Sanjay Kedhar, MD         
Sponsors and Collaborators
The New York Eye & Ear Infirmary
  More Information

No publications provided

Responsible Party: C. Michael Samson, MD, Principal Investigator, The New York Eye & Ear Infirmary
ClinicalTrials.gov Identifier: NCT01025986     History of Changes
Other Study ID Numbers: NYEE120309
Study First Received: December 3, 2009
Last Updated: December 3, 2009
Health Authority: United States: Institutional Review Board

Additional relevant MeSH terms:
Uveitis
Chorioretinitis
Uveal Diseases
Eye Diseases
Retinitis
Retinal Diseases
Choroiditis
Choroid Diseases
Uveitis, Posterior
Panuveitis

ClinicalTrials.gov processed this record on August 21, 2014