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Evaluation of a Standardised Orientation and Mobility Training in Older Adults With Low Vision

The Impact of Orientation and Mobility Training on Mobility, Participation and Quality of Life in Older Adults With Visual Impairments: a Randomised Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00946062
Enrollment
190
Registered
2009-07-24
Start date
2007-11-30
Completion date
2010-07-31
Last updated
2013-11-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Aged, Low Vision

Keywords

low vision, ophthalmology, randomised controlled trial, mobility, orientation, cane, aged

Brief summary

The purpose of this study is: 1. to develop a standardised orientation and mobility training (O&M-training) in the use of an identification/symbol cane by older adults with low vision, and; 2. to evaluate this newly developed standardised O&M-training with respect to effectiveness and feasibility in a randomised controlled trial.

Interventions

OTHERorientation and mobility training

orientation and mobility training

Sponsors

ZonMw: The Netherlands Organisation for Health Research and Development
CollaboratorOTHER
Maastricht University Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
55 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Aged 55 years or over * Low vision * Living independently in the community or in a home for older people * Able to see large obstacles and to go outside for a short walk or doing groceries * One of the following: 1. experiencing difficulties with safely crossing a street 2. experiencing difficulties with recognising acquaintances outdoors 3. willing to become recognisable as being partially sighted by using the identification cane * Written informed consent * Orientation and Mobility training (O&M-training) in the use of an identification cane

Exclusion criteria

* Cognitive impairment (a score of less than 4 on the Abbreviated Mental Test 4) * Language or hearing problems that impede completing an interview by telephone * Confinement to bed or possible nursing home admission that impede completion of the O&M-training * Permanent use of a walking aid incompatible with the use of an identification cane * Having recently received an O&M-training in the use of an identification cane and permanent use of this cane

Design outcomes

Primary

MeasureTime frame
activities of daily life (subscale of the Groningen Activity Restriction Scale (GARS))5 and 17 weeks
distance activities and mobility (subscales of the Visual Functioning Questionnaire (VFQ))5 and 17 weeks

Secondary

MeasureTime frame
health-related quality of life (EuroQol 5D (EQ5D))5 and 17 weeks
mental health and dependency (subscale of the Visual Functioning Questionnaire (VFQ))5 and 17 weeks
activities index (Frenchay Activities Index (FAI))5 and 17 weeks
symptoms of depression (depression subscale of the Hospital Anxiety and Depression Scale (HADS-D))5 and 17 weeks
concerns about falling (falls efficacy scale international (FES-I))5 and 17 weeks
feelings of anxiety (anxiety subscale of the Hospital Anxiety and Depression Scale (HADS-A))5 and 17 weeks
social support interactions (Social Support List (SSL 12-I))5 and 17 weeks

Countries

Netherlands

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 2, 2026