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Development of an intervention to treat fatigue in adults with a visual impairment.

Development of an intervention to treat fatigue in adults with a visual impairment. - Fatigue in visually impaired adults

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON42191
Enrollment
520
Registered
2015-07-16
Start date
2015-07-23
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

vision loss visual disability (visual impairment)

Interventions

Not applicable.
determinants
fatigue
intervention
visual impairment

Sponsors

Vrije Universiteit Medisch Centrum
Lead Sponsor

Eligibility

Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: - Aged 18 years and older. - Registered at one of the two low vision rehabilitation centres (ensuring a visual impairment). - Sufficient mastery of the Dutch language: participants need to be able to understand the Dutch questionnaires and be able to answer the questions in Dutch.

Exclusion criteria

Exclusion criteria: - Severe cognitive impairment: participants need to be able to understand the questionnaires to be able to participate in the study. - Comorbid diseases: cancer, chronic fatigue syndrome, multiple sclerosis and psychiatric disorders (receiving treatment for any psychiatric disorder in the last year).

Design outcomes

Primary

MeasureTime frame
The main study parameter is fatigue severity, measured by the Fatigue Assessment Scale (FAS) and the Multidimensional Fatigue Inventory (MFI).

Secondary

MeasureTime frame
Secondary variables are: - Psychological wellbeing, general perceived health and physical activity. - Vision-related quality of life and the need for recovery after work. - Perceived control and self-efficacy. - Cost evaluation associated with fatigue. Independent variables are: - Demographic data: age, gender, education level, marital status, living situation, religion and profession/daytime activities. - Disease related variables: co-morbidity, cognitive functioning and ophthalmic data.

Countries

The Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)