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A Study of Interventions to Reduce Disability From Visual Loss in Nursing Home Residents
This study is ongoing, but not recruiting participants.
First Received: July 3, 2006   No Changes Posted
Sponsors and Collaborators: Johns Hopkins University
National Institutes of Health (NIH)
Information provided by: Johns Hopkins University
ClinicalTrials.gov Identifier: NCT00348621
  Purpose

The purpose of this clinical trial is to determine if interventions within the nursing home to restore vision, or cope with visual loss, in residents with visual impairment result in improvement or less decline in mobility scores, and socialization scores, compared to residents with visual impairment in nursing homes with no such intervention.We hypothesized that nursing home residents with visual loss who receive cataract surgery, or refractive correction, or low vision aids would have have better socialization scores and mobility scores at 6 months and 12 months compared to nursing home residents with visual impairment who are advised to seek services, but have no specific program.


Condition Intervention Phase
Cataract
Refractive Error
Low Vision
Procedure: visual impairment interventions
Phase IV

Study Type: Interventional
Study Design: Treatment, Randomized, Double-Blind, Active Control, Parallel Assignment, Efficacy Study
Official Title: Clinical Trial of Interventions for Visual Loss in Nursing Home Residents

Resource links provided by NLM:


Further study details as provided by Johns Hopkins University:

Primary Outcome Measures:
  • mobility score
  • socialization score

Secondary Outcome Measures:
  • Use of psychoactive medications

Estimated Enrollment: 1600
Study Start Date: June 1999
Estimated Study Completion Date: June 2002
Detailed Description:

The goal of this project was to quantify the impact of visual acuity impairment on socialization and physical function of nursing home residents, and to determine the cost effectiveness of a visual impairment intervention program designed to enhance access to eye care services. To accomplish these aims, we enrolled a complete sample of visually impaired persons from 28 nursing homes in the Lower Eastern Shore of Maryland and Delaware. From the same facilities, we also enrolled a random sample of non-visually impaired residents, with sample size equal to the sample of visually impaired. The group of visually impaired residents was randomized (by facility) to an intervention program or “usual care” group. The intervention program facilitated the utilization of eye care services of the three main causes of visual impairment: refractive error, cataract, and low vision associated with age-related eye diseases. All study groups provided data at baseline, six and twelve months from intervention, and data on eye care utilization, hospitalizations, use of psychoactive medications and mortality collected every other month (bi-monthly). Patients had a screening test of visual acuity, using standard letter/symbol charts, and grating charts. The mental status was tested using the MiniMental State Examination.

Social function, physical function, and mobility were assessed through questionnaires asked of nursing home staff familiar with the patient, and the questions were modeled on the Minimum Data Set questions or specially designed for nursing home residents. We compare the mobility scores, and socialization scores, of nursing home residents with visual loss randomized to the intervention homes to the scores of nursing home residents with visual loss randomized to control homes.

We use the mobility and socialization scores of those without visual loss at baseline and follow up to compare with the trajectory of decline in those with visual loss.

  Eligibility

Ages Eligible for Study:   65 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Nursing homes in Eastern Shore of Maryland,within 1.5 hour drive of Salisbury MD
  • Nursing home administrators and resident committees approved the study
  • Nursing home residents:
  • Age 65 and older
  • more than 30 day length of Stay
  • Capable of acuity testing

Exclusion Criteria:

  • Nursing home residents:
  • staff assessment noted imminent death likely (within 3 months)
  • resident unable to provide informed consent and guardian not locatable
  • resident's only language was not understood by nursing staff
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00348621

Locations
United States, Maryland
Johns Hopkins University
Baltimore, Maryland, United States, 21205
Sponsors and Collaborators
Johns Hopkins University
Investigators
Principal Investigator: Sheila West Johns Hopkins University
  More Information

Publications:
Study ID Numbers: RO1AG15812
Study First Received: July 3, 2006
Last Updated: July 3, 2006
ClinicalTrials.gov Identifier: NCT00348621     History of Changes
Health Authority: United States: Institutional Review Board

Keywords provided by Johns Hopkins University:
cataract surgery
refractive correction
low vision services
nursing home
visual impairment

Study placed in the following topic categories:
Signs and Symptoms
Sensation Disorders
Vision Disorders
Eye Diseases
Cataract
Neurologic Manifestations
Lens Diseases
Refractive Errors
Vision, Low

Additional relevant MeSH terms:
Signs and Symptoms
Sensation Disorders
Vision Disorders
Eye Diseases
Cataract
Nervous System Diseases
Neurologic Manifestations
Lens Diseases
Vision, Low
Refractive Errors

ClinicalTrials.gov processed this record on September 11, 2009