Central and Peripheral Fatigue in Individuals With Parkinson's Disease - Evaluation and Training

Chang Gung University

Status: Completed

Conditions: Parkinson Disease(PD)

Treatments: Device: Electronic muscle stimulator; Other: Muscle strength training

Study type: Interventional

Funder types: Other

Identifiers

NCT01971528

100-3167A3

Details and patient eligibility

About

Fatigue is one of the most common symptoms in individuals with Parkinson's Disease (PD). Past research indicated that more than half of the individuals with PD demonstrated fatigue symptom. The severity of fatigue was also correlated to the quality of life in individuals with PD. Finding the contributions of the central and the peripheral factors to fatigue and developing an effective training program for individuals with PD are very important.

Fatigue can be categorized into peripheral or central causes. The central fatigue and voluntary activation failure originate from the decrease in motivation or the reduction of the conduction within corticospinal tracts. Long term activation failure and central fatigue will cause disuse of muscle and result in peripheral weakness and peripheral fatigue. Quantifying the weighting of central versus peripheral factors contributing to the fatigue in people with PD is important.

Most of the conventional strength and endurance training programs were based on the researches of young groups. Almost no training program was design for enhancing the voluntary activation level and relief the central fatigue. Seeking an appropriate training program to enhance central activation is very important for individuals with PD who prone to fatigue.

Previous studies have shown that increasing afferent input by peripheral electrical stimulation (ES) at sensory threshold enhanced the plasticity of contralateral primary sensory cortex, the excitability of corticospinal tracts, and the functional performance in young adults. Combining afferent input with strength training was more effective than strength training along. ES, which is easy to quantify the dose of afferent input, is a feasible method to provide such training.

The purpose of this project is to investigate the effects of the combination of ES at sensory threshold and strength training on voluntary activation in the individuals with PD.

Enrollment: 66 patients

Sex: All

Ages: 20 to 80 years old

Volunteers: Accepts Healthy Volunteers

Inclusion and exclusion criteria

Health subjects:

Exclusion Criteria:

• Musculoskeletal injuries for knee.
• Osteoporosis.
• Diabetes.

PD subjects:

Inclusion Criteria:

• Clinical diagnosis of Parkinson disease.

Exclusion Criteria:

• Musculoskeletal injuries for knee.
• Osteoporosis.
• Diabetes.
• Any peripheral or central nervous system injury or disease patients.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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66 participants in 6 patient groups

Stage 1: Health control

No Intervention group

Description:

pilot study: Establishing the central and peripheral contributing factors to the voluntary muscle strength loss during a fatiguing exercise in young and PD groups.

Stage 1: PD subjects

No Intervention group

Description:

pilot study: Establishing the central and peripheral contributing factors to the voluntary muscle strength loss during a fatiguing exercise in young and PD groups.

Stage 2: Health subjects

No Intervention group

Description:

pilot study: Finding optimal sensory stimulation parameters for PD individuals.

Stage 2: PD subjects

No Intervention group

Description:

pilot study: Finding optimal sensory stimulation parameters for PD individuals.

Stage 3: PD subjects

Experimental group

Description:

Investigating the long-term effects of combined sensory stimulating strengthening program on the activation level and central fatigue in PD individuals.

Treatment:

Device: Electronic muscle stimulator

Other: Muscle strength training

Stage 3: PD subjects (Control Subjects)

No Intervention group

Description:

Investigating the long-term effects of combined sensory stimulating strengthening program on the activation level and central fatigue in PD individuals.