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The chronic effects of hydroxy gas on people with Parkinson’s disease - a case study

Not Applicable
Conditions
Parkinson's disease
Nervous System Diseases
Registration Number
ISRCTN46799043
Lead Sponsor
niversity of Kent
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Ongoing
Sex
All
Target Recruitment
3
Inclusion Criteria

1. All participants must have a diagnosis of PD by a Neurologist or Geriatrician.
2. All participants must be at stage 2 or stage 3 on the Hoehn and Yahr (H&Y) scale. Stage 1 is too mild and stages 4 and 5 could potentially be too severe for appropriate study participation.
3. Male or female.
4. Able to attend the School of Sport and Exercise Sciences facilities
5. Able to inhale gas for 30 min, twice daily, for a period of 8 weeks
6. Participants' disease state must be stable over the past 2 months

Exclusion Criteria

1. Participants whose Parkinson’s is not controlled.
2. Participants who are at stage 1, stage 4 and stage 5 of the H&Y scale.
3. Participants who cannot consent for themselves.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Cognitive function and manual dexterity to be measured using a Purdue Pegboard Test (the three-trial administration test-retest will be used to increase reliability) at each visit (at baseline, after 2 weeks of placebo gas inhalation, after 2 weeks of hydroxy gas inhalation, after 2 weeks of placebo gas inhalation, after 2 weeks of hydroxy gas inhalation.
Secondary Outcome Measures
NameTimeMethod
<br> Measures 1-4 will be assessed at time points of: baseline, after 2 weeks of placebo gas inhalation, after 2 weeks of hydroxy gas inhalation, after 2 weeks of placebo gas inhalation, after 2 weeks of hydroxy gas inhalation.<br> 1.Transient mood measured using a Profile of Mood States (POMS)– Short Form.<br> 2. Visual attention measured using The Flanker Compatibility Task<br> 3. The burden of non-motor symptoms, including non-motor fluctuations, using the Movement Disorder Society Non-Motor Rating Scale<br> 4. Blood markers of oxidative stress, inflammation/neuro inflammation, BDNF will measured in serum or plasma derived from venous blood samples<br> 5. Levels of physical activity measured by an activity tracker worn continuously for eight weeks<br>
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