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Strength-Endurance Circuit Training in Parkinson's Disease

Strength-Endurance Circuit Training in Parkinson's Disease: Effects on Disease Severity, Physical Performance, Blood Biomarkers and Quality of Life.

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06893055
Enrollment
90
Registered
2025-03-25
Start date
2025-03-03
Completion date
2027-03-31
Last updated
2025-04-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Parkinson Disease, Idiopathic

Keywords

Parkinson Disease, Strength training, Endurance training, Physiotherapy, Irisin, Quality of Life, Physical performance

Brief summary

The goal of this clinical trial is to determine whether adding strength training to aerobic training has a comparable or greater effect on the clinical status of Parkinson's disease patients than a standalone aerobic training. \- Does combined strength-endurance circuit training provide added benefits to physical performance, disease severity, blood biomarkers, and quality of life in PD patients compared to standalone aerobic training? Participants will: * undergo outcome measurements before and after the 12-week intervention and a 3-month follow-up measurement, * visit the clinic twice a week for 1-hour training sessions. * selected patients will be given a smartwatch with a pedometer that will count their average number of steps before, during and after the training period

Interventions

OTHERStrength-Endurance Training

The intervention for the experimental Strength-Endurance group includes warm-up, three laps of strength and endurance exercises and cool-down. The training program lasts 3 months and includes two 1-hour training sessions per week, for a total of 24 sessions.

OTHEREndurance Training

The intervention for the control Endurance training group includes warm-up, three laps of endurance exercises and cool-down. The training program lasts 3 months and includes two 1-hour training sessions per week, for a total of 24 sessions.

Sponsors

General University Hospital, Prague
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* age ≥18 years * diagnosis of idiopathic Parkinson´s disease * Hoehn-Yahr Scale ≤ 2,5 * stable dopaminergic medication

Exclusion criteria

* age ≥75 years * Hoehn-Yahr Scale ≥ 2,5 * deep brain stimulation * presence of freezing * Camptocormia * inability to walk without support * inability to perform study procedures * limiting co-morbidities * attendance at training sessions below 70%

Design outcomes

Primary

MeasureTime frameDescription
Movement Disorders Society - Unified Parkinson's Disease Rating Scale (MDS-UPDRS) Part II. and III.From enrollment to the end of treatment at 12 weeks and 12 weeks after the end of treatment (Follow-up)The maximum total UPDRS score is 272, indicating the worst possible disability from PD. The minimum total score is 0, indicating no disability from PD. Improvement greater than (-4.9) points or worsening more than (+4.2) points on MDS-UPDRS II+III represent a minimal clinically important difference.

Secondary

MeasureTime frameDescription
Timed Up and Go Test (TUG)From enrollment to the end of treatment at 12 weeks and 12 weeks after the end of treatment (Follow-up)Mean TUG score for Non-falling PD patients on medication is 7.94 (2.15) seconds. MCID is 3.5 seconds.
Blood irisin levelsFrom enrollment to the end of treatment at 12 weeks and 12 weeks after the end of treatment (Follow-up)
Cardiopulmonary Exercise TestingFrom enrollment to the end of treatment at 12 weeks and 12 weeks after the end of treatment (Follow-up)
One Repetition Maximum (1RM)From enrollment to the end of treatment at 12 weeks and 12 weeks after the end of treatment (Follow-up)One Repetition Maximum in strength training is the maximum weight that can be lifted once while maintaining the correct lifting technique. It will be measured using a leg press machine for the lower extremities and a dumbbell chest press for the upper extremities.
Blood brain-derived neurotrophic factor levelsFrom enrollment to the end of treatment at 12 weeks and 12 weeks after the end of treatment (Follow-up)
Blood cytokine levelsFrom enrollment to the end of treatment at 12 weeks and 12 weeks after the end of treatment (Follow-up)
Average number of stepsAverage number of steps in the period before training (6 months), during the training period (3 months), period after training (3 months).
The Parkinson's Disease Questionnaire (PDQ-39)From enrollment to the end of treatment at 12 weeks and 12 weeks after the end of treatment (Follow-up)The minimum score is 0, while the maximum score is 100. A higher score indicates a lower QoL.

Countries

Czechia

Contacts

Primary ContactJakub Vítek, MSc.
jakub.vitek@vfn.cz+420 224 965 513

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026