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Evaluation of Ronnie Gardiner Method in Individuals With Parkinson's Disease

NCT02999997, Not applicable, Completed, University Hospital, Linkoeping

Trial 10

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

FieldValueSource
TitleEvaluation of Ronnie Gardiner Method in Individuals With Parkinson's DiseaseClinicalTrials.gov
NCT numberNCT02999997ClinicalTrials.gov
StatusCompletedClinicalTrials.gov
PhasesNot applicableClinicalTrials.gov
Enrollment51 participants, actualClinicalTrials.gov
Lead sponsorUniversity Hospital, LinkoepingClinicalTrials.gov
ConditionsParkinson DiseaseClinicalTrials.gov
InterventionsRonnie Gardiner Method (RGM)ClinicalTrials.gov
First posted2016-12-21ClinicalTrials.gov
Last updated2018-05-02ClinicalTrials.gov

Registered outcomes 19

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescriptionSource
PrimaryTimed Up and Go Cognitive (TUGcog) (motor-cognitive dual task)Change from Baseline through study completion (at 12 weeks) and at 3 months
Time in seconds to complete the following sequence: stand up from a chair, walk 3 meters, turn, walk back to the chair and sit down with the addition of counting backwards with 7 from 100, 90, 80, 70, 60, or 50. Number of errors are noted. Higher speed indicated better function.
ClinicalTrials.gov
PrimaryTimed Up and Go manual (TUG manual) (motor-motor dual task)Change from Baseline through study completion (at 12 weeks) and at 3 months
Time in seconds to complete the following sequence: stand up from a chair, walk 3 meters, turn, walk back to the chair and sit down with the additional task to carry a tray with two glasses of water. Higher speed indicates better function.
ClinicalTrials.gov
SecondaryDual-task cost (DTC)Change from Baseline through study completion (at 12 weeks) and at 3 monthsMeasuring the difference between Timed Up and Go (TUG) single task and TUG cognitive and manual respectivelyClinicalTrials.gov
SecondaryMini-BESTest (Balance Evaluation Systems Test)Change from Baseline through study completion (at 12 weeks) and at 3 monthsA balance test focusing on dynamic balance and can be conducted in 10-15 minutes.ClinicalTrials.gov
SecondaryFour Step Square Test, FSSTChange from Baseline through study completion (at 12 weeks) and at 3 months
Patient steps over four canes set-up like a cross on the floor with the tips of the canes facing together. At the start of the test, the patient stands on the upper left square (in Square 1, facing Square 2). The stepping sequence is (clockwise): Square 1, Square 2, Square 4, Square 3, return to Square 1 with the feet. Then (counterclockwise): Back to Square 3, Square 4, Square 2, and end in Square 1 with both feet.
ClinicalTrials.gov
SecondaryBerg Balance ScaleChange from Baseline through study completion (at 12 weeks) and at 3 monthsStatic and dynamic activities of varying difficulty are performed. Item-level scores range from 0-4, determined by ability to perform the assessed activity. Item scores are summed. Maximum score = 56ClinicalTrials.gov
SecondaryChair stand 30 secondsChange from Baseline through study completion (at 12 weeks) and at 3 monthsStanding up and sitting down, hands crossed over chest, as many times as possible for 30 seconds.ClinicalTrials.gov
SecondaryMontreal Cognitive Assessment (MoCA)Change from Baseline through study completion (at 12 weeks) and at 3 monthsScreening of cognitive function. License has been approved.ClinicalTrials.gov
SecondaryAuditory memory test, direct and delayedChange from Baseline through study completion (at 12 weeks) and at 3 monthsA text is read to the patient. The patient is then required to reproduce the text as exactly as possible, and then again after appr. 10 minutes.ClinicalTrials.gov
SecondarySymbol Digit Modalities Test (SDMT)Change from Baseline through study completion (at 12 weeks) and at 3 monthsA code key is presented to the patient where each code key represents a number between 1 and 9. The patient is then required to solve as many codes as possible in 90 seconds.ClinicalTrials.gov
SecondaryVictoria Stroop testChange from Baseline through study completion (at 12 weeks) and at 3 months
Colored words are presented to the patient but in a different color than the word says, eg. the word BLUE appears in the color red and the patient is required to say "red", and not read the word "blue".
ClinicalTrials.gov
SecondaryGrooved PegboardChange from Baseline through study completion (at 12 weeks) and at 3 monthsThe patient is required to move a number of metal sticks from one side to another as fast as possible. A measure of fine motor control.ClinicalTrials.gov
SecondaryTrail Making Test A and BChange from Baseline through study completion (at 12 weeks) and at 3 monthsThe patient is required to draw a line between the numbers 1 to 25 (A), and between the numbers 1 to 13 and vary to the letters A to L, i.e. 1-A-2-B-3-C, etc, without lifting the pen from the paper.ClinicalTrials.gov
SecondaryRey complex figureChange from Baseline through study completion (at 12 weeks) and at 3 monthsThe patient is required to copy a figure twice: the first time from a model in front of him/her; the second time without the model by memory only.ClinicalTrials.gov
SecondaryWHODAS 2.0BaselineA questionnaire based on the International Classification of Functioning (ICF) for assessing impairments and function.ClinicalTrials.gov
SecondaryFreezing of gait questionnaireChange from Baseline through study completion (at 12 weeks) and at 3 monthsA questionnaire with questions about freezing of gaitClinicalTrials.gov
SecondaryParkinson's disease questionnaire 39 items (PDQ-39)Change from Baseline through study completion (at 12 weeks) and at 3 monthsA questionnaire for quality of life in people with Parkinson's disease. License as been approved.ClinicalTrials.gov
SecondaryFalls Efficacy Scale International (FES-I)Change from Baseline through study completion (at 12 weeks) and at 3 monthsA questionnaire related to fear of falling.ClinicalTrials.gov
SecondaryActigraphy with GeneActiv ArmbandChange from Baseline through study completion (at 12 weeks) and at 3 months
Actigraphy is a method to evaluate physical activity in a research person´s normal life. GeneActiv is used to record number of steps daily but also time spent lying and standing which will give information about the activity.
ClinicalTrials.gov

Outcomes 0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured asSource

Results by group 0

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnitsSource

Participant flow 0

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits countedSource

Adverse events 0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

TypeEventOrgan systemGroupAffectedAt riskEventsSource

Adverse event totals 0

The totals the trial posted for each group.

TotalGroupAffectedAt riskSource

Papers 2

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
36602886DERIVEDPubMed
38588457DERIVEDPubMed

Grants 0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

ProjectTitlePrincipal investigatorsOrganizationFunderFiscal yearsSource

Trial comparisons 0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

ComparisonSource

Tests 5

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

TestNamed asSource
Complex Figure Copy and RecallSecondary outcomeConductCognition
Stroop Color-Word TestSecondary outcomeConductCognition
Symbol CodingSecondary outcomeConductCognition
Trail Making Test ASecondary outcomeConductCognition
Trail Making Test BSecondary outcomeConductCognition

Source 5

FieldValueSource
Releasetrials-2026-11-12-0.4.0ClinicalTrials.gov
Release manifest SHA-2560f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4ClinicalTrials.gov
Registry capture2026-11-12ClinicalTrials.gov
Results copy, AACT2026-03-23ClinicalTrials.gov
NIH clinical studies file2026-11-13ClinicalTrials.gov

The same record as JSON

Release trials-2026-11-12-0.4.0

ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299 ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

ClinicalTrials.gov: none stated ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

NIH RePORTER's clinical studies and project files: Public domain (NIH RePORTER)