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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01121627
Other study ID # K-10-0036-ctil
Secondary ID
Status Completed
Phase N/A
First received May 10, 2010
Last updated August 21, 2015
Start date July 2010
Est. completion date April 2012

Study information

Verified date August 2015
Source Clalit Health Services
Contact n/a
Is FDA regulated No
Health authority Israel: Ministry of Health
Study type Interventional

Clinical Trial Summary

Parkinson's Disease (PD) is a neurodegenerative, progressive illness. It is a multi-system disease that influences not only the motor but also the cognitive and autonomic systems. The main cognitive impairment in individuals with PD is found in executive function (EF). EF is defined as a set of cognitive skills necessary for planning, monitoring and executing sequences of complex activities.

The primary study hypothesis is that computer-based training aimed at improving executive function will have a beneficial effect on gait functions.


Description:

Parkinson Disease (PD) is a neurodegenerative, progressive illness. It is a multi-system disease that influences not only the motor but also the cognitive and autonomic systems. The main cognitive impairment in individuals with PD is found in executive function (EF). EF is defined as a set of cognitive skills necessary for planning, monitoring and executing sequences of complex activities. Previous studies have revealed some relation between cognitive states and physical functions in healthy adults. Few studies have examined the effect of computer-based cognitive training on various populations. These studies showed a positive emotional-cognitive effect in those populations. This type of intervention plan was also applied to PD patients. However, there are no reports on the effect of intentional cognitive training on gait functions. The purpose of the study is to assess whether cognitive training, designed to improve EF ability, can also improve gait function in PD patients.


Recruitment information / eligibility

Status Completed
Enrollment 30
Est. completion date April 2012
Est. primary completion date April 2012
Accepts healthy volunteers No
Gender Both
Age group 50 Years to 80 Years
Eligibility Inclusion Criteria:

1. Idiopathic PD.

2. Aged 50-80, living in north region of Israel.

3. Receive regular medications for PD.

4. Not suffering from irregular cognitive disturbance or MMSE<25.

5. Measured 1-3 on the Hoehn & Yahr scale.

6. Have access to a computer and the ability to operate it.

Exclusion Criteria:

1. Brain operation, including DBS transplant.

2. History of orthopedic problems that can impair gait (hip/knee fractures and back problems).

3. Orthopedic operation on lower limbs performed no later than six months prior to the beginning of the study.

4. Unbalanced general health: uncontrolled diabetes or blood pressure, etc.

5. Inability to walk independently.

6. Immunodeficiency diseases, active cancer, ischemic diseases.

7. Vision impairment, partial/full blindness.

8. Having participated in similar research or cognitive assessment during the previous year.

9. Have received cognitive or gait training under physical therapy or other programs.

Study Design

Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Other:
Computerized cognitive training
A 12 week computerized cognitive training at home with the Attengo™ software program.

Locations

Country Name City State
Israel Clalit Health Services, Haifa and Western Galilee District Haifa

Sponsors (2)

Lead Sponsor Collaborator
Clalit Health Services Tel-Aviv Sourasky Medical Center

Country where clinical trial is conducted

Israel, 

References & Publications (1)

Milman U, Atias H, Weiss A, Mirelman A, Hausdorff JM. Can cognitive remediation improve mobility in patients with Parkinson's disease? Findings from a 12 week pilot study. J Parkinsons Dis. 2014;4(1):37-44. doi: 10.3233/JPD-130321. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Gait Function At enrollment eligible individuals will undergo a thorough baseline assessment using a predefined set of tests and performance measurements. Within a week after enrollment each individual will receive guided training on the use of the intervention tool, the Attengo™ software program. Thereafter they will train at their homes, at least three times a week, for a period of 12 weeks. Follow up assessments will be performed within a week of the end of the training period and 4 weeks thereafter to check for long-term cognitive and motor changes. 18 weeks No
Secondary Executive function At enrollment eligible individuals will undergo a thorough baseline assessment using a predefined set of tests and performance measurements. Within a week after enrollment each individual will receive guided training on the use of the intervention tool, the Attengo™ software program. Thereafter they will train at their homes, at least three times a week, for a period of 12 weeks. Follow up assessments will be performed within a week of the end of the training period and 4 weeks thereafter to check for long-term cognitive and motor changes. 18 weeks No
Secondary Quality of life. At enrollment eligible individuals will undergo a thorough baseline assessment using a predefined set of tests and performance measurements. Within a week after enrollment each individual will receive guided training on the use of the intervention tool, the Attengo™ software program. Thereafter they will train at their homes, at least three times a week, for a period of 12 weeks. Follow up assessments will be performed within a week of the end of the training period and 4 weeks thereafter to check for long-run cognitive and motor changes. 18 weeks No
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