Actively Recruiting
Effect of Training and Use of Cane on Gait in Individuals With Parkinson's Disease
Led by Federal University of Minas Gerais · Updated on 2025-05-02
26
Participants Needed
1
Research Sites
69 weeks
Total Duration
On this page
Sponsors
F
Federal University of Minas Gerais
Lead Sponsor
F
Fundação de Amparo à Pesquisa do estado de Minas Gerais
Collaborating Sponsor
AI-Summary
What this Trial Is About
Introduction: Although individuals with Parkinson's disease (PD) commonly use assistive devices, the effects of these devices on gait remain poorly understood. Furthermore, previous studies on this topic only investigated the immediate effects of device usage, and the investigated outcomes were predominately performance-based neglecting participant-centered outcomes. Objective: To investigate the effect of cane training and use on gait speed (primary outcome), gait confidence, cadence, step length, functional mobility, freezing of gait, fear of falls and satisfaction with the use of a cane (secondary outcomes) in individuals with PD. Methods: A double-blind, randomized controlled trial with intention-to-treat and per-protocol analysis will be carried out. A total of 26 individuals with PD will be recruited based on the following inclusion criteria: age ≥ 40 years, diagnosis of idiopathic PD, classification between stages II to IV on the modified Hoehn \& Yahr Scale, stable use of anti-parkinsonian pharmacological therapy, ability to walk independently with a walking speed ≤ 1.1 m/s (defined to screen individuals with gait impairments), and ability to use a single-point cane during walking without regular use of any type of assistive device since the diagnosis of PD. Participant will be randomly divided into two groups that will receive: (1) cane training and use (experimental group) or (2) global stretches and health education (time and attention-controlled group). The intervention will be provided in four sessions lasting 40 minutes each, spaced over 15 to 22 days. Additionally, individuals will be instructed to use a cane (experimental group) or perform stretching exercises (time and attention-controlled group) daily, starting from the first day of training. Assessments will be conducted at the beginning of the study (week 0), post-intervention (after the 3-week intervention), and one month after the cessation of the intervention (8-week follow-up). The primary outcomes is gait speed. Secondary outcomes include gait confidence, cadence, step length, functional mobility, freezing of gait, fear of falls, and satisfaction with the use of a cane. Between-group differences will be measured using a two-way repeated measures ANOVA, considering baseline, post-intervention, and follow-up assessments, following both intention-to-treat and per-protocol approaches (α=0.05). Conclusions: The results of the present study will provide information about the effects of cane training and use on the gait of individuals with PD who will have the opportunity to use the cane in their real-life context.
CONDITIONS
Official Title
Effect of Training and Use of Cane on Gait in Individuals With Parkinson's Disease
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Diagnosis of idiopathic Parkinson's disease confirmed by a neurologist
- Classified between stages II to IV on the modified Hoehn & Yahr Scale
- Using stable anti-parkinsonian medication for at least 6 months
- Able to walk independently in a 14-meter corridor with walking speed of 1.1 m/s or less
- Able to correctly and safely use a single-point cane and not a regular user of assistive devices since Parkinson's diagnosis
You will not qualify if you...
- Cognitive impairment as assessed by the Mini Mental State Examination
- Use of deep brain stimulation
- Any other neurological, cardiopulmonary, or musculoskeletal condition that could affect test performance
AI-Screening
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Trial Site Locations
Total: 1 location
1
Federal University of Minas Gerais
Belo Horizonte, Minas Gerais, Brazil, 31270901
Actively Recruiting
Research Team
C
Christina DCM Faria, Doctor
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
DOUBLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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