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Parkinson AKTIV - Non-pharmacological Treatments in an Innovative Parkinson's Network

Parkinson AKTIV - Non-pharmacological Treatments in an Innovative Parkinson's Network- Evaluates the Efficacy of an Online Platform That Allows Neurologists and Therapists to Exchange Therapy Recommendations Regarding Their Patients With Parkinson's Disease (PwP), Communicate Assessments and Plan Physical Therapy, Occupational Therapy as Well as Speech and Swallowing Therapy

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05251298
Acronym
ParkinsonAKTIV
Enrollment
370
Registered
2022-02-22
Start date
2021-11-28
Completion date
2024-10-31
Last updated
2023-04-20

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

Conditions

Parkinson Disease

Keywords

Activities of Daily Living, Disease Management, Quality of Life, Rehabilitation, Patient-Centered Care, Delivery of Health Care, Integrated Care

Brief summary

The purpose of this study is to evaluate the efficacy of an online platform that allows neurologists and therapists to exchange therapy recommendations, communicate assessments and plan physical therapy, occupational therapy as well as speech and swallowing therapy for their patients.

Detailed description

The aim of this study is to enroll 185 patients in the intervention group and 185 patients in the control group. Patients in the intervention group come from the same region (Münsterland), the control group will consist of patients outside this region. The patients in the intervention group undergo therapies planned and coordinated through the online platform for 12 months. The patients in the intervention group will be evaluated using the PDQ-39, UPDRS, H&Y as well as Schwab & England. The patients in the control group will be evaluated using the PDQ-39.

Interventions

OTHERCoordination through the online platform JamesAKTIV

Coordination of the treatment through the online platform JamesAKTIV that allows neurologists and therapists to select specialised therapies for the predominant symptoms of the patients and communicate easily about problems during the treatment

Sponsors

privates Institut für angewandte Versorgungsforschung GmbH
CollaboratorUNKNOWN
AOK PLUS
CollaboratorINDUSTRY
University Hospital Muenster
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
30 Years to No maximum
Healthy volunteers
No

Inclusion criteria

(Intervention Group): * Idiopathic Parkinson's Disease with pharmacological treatment * 30 years old or older * place of residence: Münsterland, Tecklenburger Land, Kreis and Stadt Osnabrück * sufficient knowledge of the German language, should be able to understand the consent form

Exclusion criteria

* severe cognitive deficits * Atypical Parkinsonian Disorders * participation in other studies

Design outcomes

Primary

MeasureTime frameDescription
Change in Quality of Life measured by PDQ 39Change from Baseline PDQ 39 at 12 monthsThe Parkinson's Disease Questionnaire (PDQ-39, max. score of 100 indicates the worst quality of life)

Secondary

MeasureTime frameDescription
Change in Health-related resource use in the elderly population, assessed by FIMAChange from Baseline FIMA at 12 monthsFIMA stands for Questionnaire concerning Health-related resource use in the elderly population and is a German questionnaire assessing the Health-related resource use in the elderly population
Change in disease severity measured by UPDRSChange from Baseline UPDRS at 12 monthsUPDRS - Unified Parkinson's Disease Rating Scale, max. score of 199 points indicates the worst outcome
Change in disease severity measured by Hoehn & YahrChange from Baseline UPDRS at 12 monthsHoehn & Yahr is a simple scale that describes disease severity on a scale of 0-5, with 5 indicating severe disability
Change in mobility, measured by Schwab- & England-ScaleChange from Baseline Schwab-&England-Scale at 12 monthsSchwab- & England-Scale assesses the capabilities of people with impaired mobility. The scale uses percentages with 100% indicating full independence.

Countries

Germany

Contacts

Primary ContactTessa Huchtemann, Medical Degree
Tessa.Huchtemann@ukmuenster.de004915254956565
Backup ContactTobias Warnecke, Medical Degree, PhD
Tobias.Warnecke@ukmuenster.de00492518345314

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 11, 2026