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Comparison of the effects of Mental Practice protocols for Functional Mobility and Risk of Falls in Parkinson's disease

Mental Practice protocols for Functional Mobility and Risk of Falls in Parkinson's disease: A Randomized trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-23nyf4
Enrollment
Unknown
Registered
2018-01-08
Start date
2017-10-01
Completion date
Unknown
Last updated
2025-10-27

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

Conditions

Parkinson Disease

Interventions

Patients will be randomly divided into an audio-guided Mental Practice Group and a video-guided mental practice group. All patients will undergo 15 sessions of physiotherapy at a frequency of twice a
Other
E02.779

Sponsors

Universidade Federal de Pernambuco
Lead Sponsor
Hospital das Clínicas da Universidade Federal de Pernambuco
Collaborator

Eligibility

Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Patients with clinical diagnosis of idiopathic Parkinson's disease according to Ordinance No. 228/2010 of the Ministry of Health of Brazil; Both sexes; Patients aged 18-80 years; Stage 1 to 3 of Hoehn and Yahr's original scale.

Exclusion criteria

Exclusion criteria: Other neurological diseases; orthopedic, rheumatic and / or vascular pathology, with moderate or severe functional restriction in one or both lower limbs; uncontrolled hypertension and / or cardiac or respiratory disease that limits the execution of the protocol; with lowering of the cognitive level; with medical restriction to perform exercises; unable to perform the motor imagination, in physical therapy or occupational therapy for 3 months or more; with moderate to severe depression; with visual and auditory deficits that do not guarantee a good participation in the protocol; after deep brain stimulation surgery; with vestibular alterations; with lack of sensitivity in the lower limbs; users of orthosis for lower limbs; User of prosthetics; with edemas in the lower limbs and amputees

Design outcomes

Primary

MeasureTime frame
Improvement in gait, evaluated by the 10-meter walk test, with a reduction of at least 10% in the number of steps, 5% reduction in cadence and a 10% increase in walking speed. Data collected 1 day before the intervention and 1 day after the intervention.

Secondary

MeasureTime frame
5% reduction in fear of falls, measured by the history of falls questionnaire, data collected 1 day before the intervention and 1 day after the intervention

Countries

Brazil

Contacts

Public ContactLiliane Pereira da Silva

Universidade Federal de Pernambuco

pereiradasilva20@hotmail.com+55(81)984527989

Outcome results

None listed

Source: REBEC (via WHO ICTRP)