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Study on the proposal for pre-rehabilitation work and health-related quality of life of adults with visual impairment who are on the waiting list

Rehabilitation and health-related quality of life of adults with visual impairment: clinical trial of a pre-rehabilitation proposal with a waiting list

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-62ghfw4
Enrollment
Unknown
Registered
2025-11-14
Start date
2025-08-18
Completion date
Unknown
Last updated
2025-11-17

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

Conditions

Visual Impairment

Interventions

This is a pragmatic randomized controlled clinical trial involving two groups of people with visual impairments (low vision or blindness) selected from the waiting list of the Benjamin Constant Instit
s Rehabilitation Program (MEC/RJ). One group will participate in the intervention—&quot
pre-rehabilitation&quot
(n=50) and the other will be the control group (n=50). The intervention group will participate in introductory educational and therapeutic workshops led by education and health professionals who are
s rehabilitation team, focusing on areas aimed at improving independence, autonomy, and coping with visual loss. Participants in the control group will attend a workshop on the rights of people with d

Sponsors

Escola Nacional de Saúde Pública Sérgio Arouca/ Fundação Oswaldo Cruz
Lead Sponsor
Centro Universitário de Valença/Fundação Educacional Dom André Arcoverde
Collaborator

Eligibility

Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: individuals aged 18 or older; both genders; registered on the waiting list for the Benjamin Constant Institute Rehabilitation Program; never participated in any rehabilitation program for visual impairment; blindness in both eyes; blindness in one eye and low vision in the other eye; low vision in both eyes

Exclusion criteria

Exclusion criteria: individuals living with other severe associated disabilities; pregnant women; patients with chronic illnesses requiring hospitalization

Design outcomes

Primary

MeasureTime frame
Evaluate scores for Life Activities Daily verified by the method of measuring a dimension of the NEI VFQ-25 instrument.

Secondary

MeasureTime frame
Evaluate utility using the instrument EQ-5D-3L and the scores of the other dimensions of the NEI VFQ-25.

Countries

Brazil

Contacts

Public ContactSonia Regina Rocha

Instituto Benjamin Constant - Ministério da Educação

soniagomes@ibc.gov.br+55(21)34784560

Outcome results

None listed

Source: REBEC (via WHO ICTRP)