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Strength Training and Different Subtypes of Parkinson´s Disease

Not Applicable
Completed
Conditions
Parkinson Disease
Interventions
Other: Progressive resistance exercise
Other: Physical Activity
Registration Number
NCT02966600
Lead Sponsor
University of Oviedo
Brief Summary

The aim of this randomized controlled trial was to assess the impact of progressive resistance exercise (PRE) in PD patients with akinesia and rigidity (AR-subtype). The investigators hypothesized the intervention would have a beneficial effect on the study outcomes.

Detailed Description

Twenty-eight patients with PD AR-type of both sexes, were recruited for this trial. Each participant were assigned randomly to either intervention (N=13) or control (N=15) group.

The intervention group participated in sixteen PRE training sessions for eight weeks: two sessions per week on non-consecutive days, sixty-seventy min each one. The control group followed their usual weekly physical activity routine.

All patients underwent antrophometrical and neuromuscular function assessment (CoP measurements -primary outcomes- and the Ten-Meters Walk Test -TMWT- -secondary outcomes-). In addition, they were asked to provide ratings for the Spanish validated versions of the the Freezing of Gait Questionnaire (FOG-Q, 6-item version) -secondary outcomes-, the 39-item Parkinson ́s disease Questionnaire (PDQ39) -secondary outcomes- and the MDS-UPDRS -secondary outcomes-. Additionally, ratings of perceived exertion (RPE) (Borg \>6-20 scale) - secondary outcomes-, were recorded at the end of each PRE training session. Tests were carried out at three times: pre-test (before the training program), post-test (eight weeks after pre-tests, at the end of the training period), and four weeks after the post-test (re-test).

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
28
Inclusion Criteria
  • Diagnosed with PD AR-type and Hoehn and Yahr Scale 1-2, (H&Y)
  • Do not express any type of dementia
  • Able to stand for two min without assistance;
  • Able to walk ten metres without assistance.

Exclusion criteria:

  • To suffer a neurological disease other than PD.
  • Do not meet some of the inclusion criteria.
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Exclusion Criteria

Not provided

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Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Progressive resistance exercise (PRE)Physical ActivityProgressive resistance exercise (PRE) in akinetic-rigid Parkinson's disease patients. Intervention included sixteen PRE training sessions for eight weeks: two sessions per week on non-consecutive days, sixty-seventy min each one.
Progressive resistance exercise (PRE)Progressive resistance exerciseProgressive resistance exercise (PRE) in akinetic-rigid Parkinson's disease patients. Intervention included sixteen PRE training sessions for eight weeks: two sessions per week on non-consecutive days, sixty-seventy min each one.
Primary Outcome Measures
NameTimeMethod
Static posturography through the centre of pressures measurements (CoP).Eight weeks
Secondary Outcome Measures
NameTimeMethod
The patient- perceived quality of life.Eight weeks
Gait.Eight weeks
Freezing of gait.Eight weeks
The Movement Disorders Society-Unified Parkinson ́s Disease Rating Scale. (MDS-UPDRS).Eight weeks

Trial Locations

Locations (1)

University School of Sports Medicine, University of Oviedo, Spain.

🇪🇸

Oviedo, Asturias, Spain

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