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Prevention of Disability: Proposal for a Guidance Manual for Leprosy Patients

Proposal Evaluation and Intervention Through Prevention of Disability in Leprosy Patients

Status
Completed
Phases
Phase 1
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01006759
Enrollment
55
Registered
2009-11-03
Start date
2007-01-31
Completion date
2009-08-31
Last updated
2009-11-03

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

Conditions

Disability Evaluation, Leprosy, Quality of Life

Keywords

Leprosy, Disability Evaluation, Quality of Life, Sensation

Brief summary

Leprosy is an infectious disease of slow evolution, manifested primarily by signs and symptoms dermatoneurological with skin lesions and peripheral nerve, especially in the eyes, hands and feet. The prevention of disability is essential for the control of complications. Objective: To evaluate the physical and functional status of hands, feet and eyes, for the appearance and evolution of sensory and motor deficiencies and classification of disability (WHO) of a group of leprosy patients to compare and monitor the result treatment on the progression of neuropathy and recurrence of reactions. Methodology: We performed initial physical therapy evaluation and final, after 12 months. We conducted a clinical trial of a series of 26 cases evaluated with newly diagnosed leprosy, treated by standard medication. There were used methods of qualitative and quantitative. An illustrated manual of guidelines was especially developed for this study.

Detailed description

assessment methods of qualitative and quantitative: inspection of eyes, hands and foot, manual motor function, grip and pinch dynamometry,threshold test, SF 36 quality of life questionnaire. Intervention: illustrated guidelines, exercises, orthoses, orientation Goals: disability prevention

Interventions

OTHERexercise and orientation

guidances for prevention of disability in leprosy with focus on hands, eyes and feet.

Sponsors

Conselho Nacional de Desenvolvimento Científico e Tecnológico
CollaboratorOTHER_GOV
University of Sao Paulo
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
PREVENTION
Masking
NONE

Eligibility

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

Inclusion criteria

* The patients in this project were diagnosed and referred by the dermatology to do the physical-functional evaluation and physiotherapy. We selected patients aged 18 years and both sexes, even with comorbidities, since diagnosed and treated. In accepting to participate in the research, signed a consent form

Exclusion criteria

* Those patients who refused to sign the consent form and those who did not attend the evaluations

Design outcomes

Primary

MeasureTime frame
classification of disability for Leprosy(WHO)1 year

Secondary

MeasureTime frame
classification of disability for Leprosy(WHO), grip strength and threshold sensibilityafter 1 year

Countries

Brazil

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026