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

NCT ID: NCT05251298

Last Updated: 2023-04-20

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

370 participants

Study Classification

INTERVENTIONAL

Study Start Date

2021-11-28

Study Completion Date

2024-10-31

Brief Summary

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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

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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.

Conditions

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Parkinson Disease

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

HEALTH_SERVICES_RESEARCH

Blinding Strategy

NONE

Study Groups

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Intervention group

Patients in the intervention group come from the same region (Münsterland) and will undergo therapies coordinated through the online platform.

Group Type ACTIVE_COMPARATOR

Coordination through the online platform "JamesAKTIV"

Intervention Type OTHER

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

Control group

Patients in the control group will undergo their usual therapies as prescribed by their neurologists.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Coordination 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

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* 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
Minimum Eligible Age

30 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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privates Institut für angewandte Versorgungsforschung GmbH

UNKNOWN

Sponsor Role collaborator

AOK PLUS

INDUSTRY

Sponsor Role collaborator

University Hospital Muenster

OTHER

Sponsor Role lead

Responsible Party

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Dr. Tobias Warnecke

Professor Dr. Tobias Warnecke

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Universitätsklinikum Münster, Klinik für Neurologie

Münster, North Rhine-Westphalia, Germany

Site Status RECRUITING

Countries

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Germany

Central Contacts

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Tessa Huchtemann, Medical Degree

Role: CONTACT

004915254956565

Tobias Warnecke, Medical Degree, PhD

Role: CONTACT

00492518345314

Facility Contacts

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Tessa Huchtemann, Medical Degree

Role: primary

004915254956565

References

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Achtert K, Huchtemann T, Altendorf M, Kerkemeyer L, Haring M, Lummer C, Frenz L, Becking T, Friedmann J, Mildner P, Schwarze K, Steinhaus L, Amelung V, Warnecke T. Design and implementation of ParkinsonAKTIV: an interventional study to evaluate the effectiveness of a novel online platform to guide quickcard-based treatment decisions. Neurol Res Pract. 2023 Jun 1;5(1):23. doi: 10.1186/s42466-023-00249-5.

Reference Type DERIVED
PMID: 37259124 (View on PubMed)

Other Identifiers

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01NVF19002

Identifier Type: OTHER_GRANT

Identifier Source: secondary_id

2021-356-f-S

Identifier Type: -

Identifier Source: org_study_id

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