Expectation and Response to Levodopa and Acupuncture in Parkinson's Disease

Oregon Health & Science University (OHSU)

Status: Completed

Conditions: Parkinson's Disease

Treatments: Behavioral: Levodopa or acupuncture

Study type: Interventional

Funder types: Other; NIH

Identifiers

NCT00692328

U19AT002656-02 (U.S. NIH Grant/Contract)

AT002656-02

Details and patient eligibility

About

To investigate how levodopa and acupuncture affect fatigue and muscle function in people who suffer from Parkinson's disease. Subjects may choose to participate in levodopa or acupuncture part, or both. Study procedures include an exercise protocol, transcranial magnetic stimulation (a non-invasive type of brain stimulation that cause small muscle twitch), a blood draw, and personality surveys.

Full description

Subjects will answer surveys, have their blood drawn, undergo TMS and perform an exercise. The TMS/exercise task will measure fatigue and muscle response. The surveys will describe personality and measure fatigue. The CTRC will do genotype studies on the blood to look for genetic differences. Each subject is eligible to receive both study treatment types (levodopa and acupuncture). Depending upon the study treatment type they choose, each subject will be randomly assigned to one of six possible subject groups:

Ia. Full expectancy; levodopa: Subjects will be told that they are taking levodopa.

Ib. Half expectancy; levodopa: Subjects will be told that they have 50% chance of receiving levodopa or placebo.

Ic. No expectancy; levodopa: Subjects will be told that they are receiving placebo levodopa.

IIa. Full expectancy; acupuncture: Subjects will be told that they are receiving real acupuncture.

IIb. Half expectancy; acupuncture: Subjects will be told that they have 50% chance of receiving real or sham-acupuncture.

IIc. No expectancy; acupuncture: Subjects will be told that they are receiving sham-acupuncture.

Subjects will attend four visits for the levodopa part and/or three visits in the acupuncture part. On the first visit, subjects will answer questionnaires and have samples of their blood collected. On the other visits, subjects will undergo TMS while they perform a repetitive exercise task. Subjects will then either wait for 30 minutes or receive the investigative intervention that they have been randomly assigned for that particular visit, and then repeat the TMS/exercise task.

Enrollment: 63 patients

Sex: All

Ages: 18 to 80 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Clinical diagnosis of Parkinson's disease
• Able to withdraw Parkinson's disease medication for 12 hours prior to a study visit
• Must be currently using levodopa to qualify for the levodopa part of the study

Exclusion criteria

• History of seizures
• Presence of any metal in the body, including DBS stimulators, pacemakers, metal plates or pins
• Severe cognitive deficits or psychosis
• Evidence of any clinically unstable disease, such as cancer, HIV/AIDS; unstable heart condition or other conditions that might require hospitalization
• Evidence of another neurological disease, such as multiple sclerosis, amyotrophic lateral sclerosis, or Huntington's disease

Trial design

Primary purpose: Basic Science

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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63 participants in 3 patient groups, including a placebo group

1

Active Comparator group

Description:

The subjects will be told they receive levodopa or acupuncture.

Treatment:

Behavioral: Levodopa or acupuncture

2

Placebo Comparator group

Description:

The subjects will be told they receive placebo/sham levodopa or acupuncture.

Treatment:

Behavioral: Levodopa or acupuncture

3

Experimental group

Description:

The subjects will be told they have 50% chance of receiving real or placebo/sham levodopa or acupuncture.

Treatment:

Behavioral: Levodopa or acupuncture