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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT03811613
Other study ID # #08/18
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date January 29, 2018
Est. completion date March 30, 2018

Study information

Verified date January 2019
Source University of Oviedo
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study aimed to assess the effects of transcranial photobiomodulation in patients with Parkinson's disease (PD).


Description:

Thirty-five patients with idiopathic PD were randomly assigned to a photobiomodulation (n=17, [mean±SD] 72±7 years) or sham group (n=18, 70±8 years) during 9 weeks (2 sessions/week). The primary endpoint was the motor portion of the Movement Disorders Society-United PD Rating Scale. Secondary endpoints were the Scales for Outcomes in PD, static posturography, walking ability (ten-meter walk test [TMWT]) and functional mobility (timed up and go [TUG] test).


Recruitment information / eligibility

Status Completed
Enrollment 35
Est. completion date March 30, 2018
Est. primary completion date March 30, 2018
Accepts healthy volunteers No
Gender All
Age group N/A and older
Eligibility Inclusion Criteria:

- Having been diagnosed with idiopathic PD.

- Stage 1-2 on the Hoehn and Yahr Scale.

- Having no neurological condition other than PD.

- Being able to stand for 2 minutes and walk 10 meters without assistance.

- Having no severe dyskinesias or "ON-OFF" phases.

Exclusion Criteria:

- Do not follow inclusion criteria.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Transcranial photobiomodulation
Photobiomodulation was administered using red light-emitting diodes (LEDs) with a 670-nm wavelength (which has proven to penetrate the skull)

Locations

Country Name City State
Spain Department of Physical Education and Sport, University of León León Castilla Y León
Spain University School of Sports Medicine, University of Oviedo, Spain. Oviedo Asturias

Sponsors (1)

Lead Sponsor Collaborator
University of Oviedo

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary The motor portion of the MDS-UPDRS. The motor portion (part III) Movement Disorders Society-Unified PD Rating Scale. It assesses the motor signs of Parkinson´s disease (minimum and maximum score is 0 and 76 points respectively -the higher score, the higher movement disorder and vice versa-). 9 weeks
Secondary Motor function The Spanish-validated version of the Short Parkinson's Evaluation Scale (SPES)/Scales for Outcomes in PD (SCOPA). It measures the Parkinson´s disease patients motor function (minimum and maximum score is 0 and 63 points respectively -the higher score, the worse motor function and vice versa-). 9 weeks
Secondary Static posturography The centre of pressure (CoP) parameters (these CoP parameters; Length in mm, Area in mm2 and Speed in m/s are combined to report the static posturography). 9 weeks
Secondary Walking speed Ten-meter walk test 9 weeks
Secondary TUG Timed up and go test 9 weeks
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