Transforming Parkinson's Care With Predictive Algorithms (TechHealthPD)

November 27, 2025 updated by: University Ramon Llull

Revolutionizing Patient Care and Lifestyle Through Predictive Algorithms in Parkinson's Disease

Lifestyle interventions can alleviate Parkinson's Disease (PD) symptoms and delay disease progression. The novelty of this project lies in the development of an innovative smart platform that utilizes artificial intelligence (AI) and predictive models to offer a groundbreaking solution that not only prevents disease progression but also significantly improves the well-being of patients with PD. For this, the technological smart platform will encompass 50 clinical variables, and a comprehensive range of other 50 supplementary variables, validated in a database with more than 1500 patients. The smart platform will include a user-friendly interface with different user profiles and a scalable back end with AI-based monitoring and prediction modules. This will offer primary prevention, early detection, and ongoing monitoring by specialized medical professionals at home and in hospitals.

Study Overview

Status

Not yet recruiting

Conditions

Intervention / Treatment

Detailed Description

Parkinson's Disease (PD) is the second most prevalent neurodegenerative disorder and the most common disorder that affects motor coordination, affecting 2% of the population above 65 years old and 4% in the population above 80 years old. Patients diagnosed with PD suffer with severe motor and non-motor symptoms. Typical motor symptoms include resting tremor or rigidity, slowness in voluntary movements called bradykinesia, difficulty in pronunciation when speaking, while non-motor symptoms could be sleep, cognitive and autonomic function disorders. PD not only disrupts motor function but also significantly influences the quality of life, sleep patterns, cognitive aspects, and mood of those living with the condition. While there is no cure for PD, certain treatments such as medication, surgery, and interdisciplinary approaches can effectively address and manage PD-associated symptoms. Given the diversity of treatments and the diverse impact of motor and non-motor symptoms on daily functioning, there's a growing need for more comprehensive interventions. Numerous studies have explored the impact of lifestyle interventions, such as physical activity (PA) on various aspects of PD, suggesting that patients with PD might benefit from PA in a number of ways, from general improvements in health to disease-specific effects and potentially, disease-modifying outcomes. To this aim, we conducted a randomized double-blind clinical trial conducted to study the effects of PA on mitochondrial function in skin fibroblasts in patients with PD (NCT05963425). This was an intervention study, with twenty-four patients, that were randomly assigned into three groups (8 patients/group). The first group performed basic physical training (BPT) based on strength and resistance, the second group performed BPT combined with functional exercises (BPTFE) with cognitive and motor training, and the third group did not carry out any activity program, serving as control. The PA interventions lasted 60 minutes, with a frequency of 3 times a week, during 16 weeks. The main objective was to assess the effects of PA on mitochondrial function, and its effects on a wide variety of clinical factors, such as motor function, quality of life, sleep, cognitive aspects, and mood.

Building on the holistic insights from the previous study, this project sets out to create a technological smart platform, utilizing artificial intelligence (AI), to foster healthy habits and optimal clinical management among PD population. Technological platforms emerge as instrumental tools in transforming the landscape of PD management. These platforms can facilitate continuous monitoring and tailored interventions that integrate, for example, lifestyle-embedded exercise programs. However, while technological interventions have shown promise in promoting healthy habits, there is limited research on the integration of AI for personalized interventions in the context of PD. Models developed to date have several key limitations including use of only one single feature (i.e. motor symptoms), model assumptions that patients follow a fixed progression, or not accounting for both positive and negative effects of symptomatic therapies for PD. Herein, we address the current limitations and propose a holistic approach based on an AI model that provides professionals, patients and carers with a smart platform capable of promoting healthy habits and optimizing clinical aspects. Herein, we recognize the importance of PA along with other healthy habits for PD patients by incorporating more than 50 other variables from the Movement Disorder Society-Sponsored Revision of the Unified Parkinson's Disease Rating Scale (MDS-UPDRS), a comprehensive clinical tool used to assess both motor and non-motor symptoms in PD patients, divided into four parts that evaluate daily living experiences, motor examination, and therapy-related motor complications. Importantly, the data collected will be validated with the Parkinson's Progression Markers Initiative (PPMI), a landmark study with more than 1500 patients designed to identify biomarkers of PD progression, enhancing the reliability and applicability of our findings. The successful execution of this project will culminate in an integrated solution that combines web and mobile interfaces, enhancing the overall accessibility and effectiveness of PD diagnostic and monitoring capabilities. The proposed AI-based smart platform has significant social implications, primarily in improving the quality of life for PD patients by addressing both motor and non-motor symptoms. It fosters a more comprehensive and personalized approach to PD management, moving beyond the limitations of current treatment methods, which often focus on singular aspects of the disease. By incorporating a wide range of variables from a well-established clinical database, the platform aims to deliver tailored interventions that promote healthy habits and optimize clinical outcomes. Additionally, the platform's use of AI for continuous monitoring and adaptive interventions will empower patients and caregivers, providing real-time support and reducing the burden on healthcare systems. This represents a shift towards more patient-centered, proactive care, potentially improving disease progression management and quality of life for the aging population affected by PD. In conclusion, the comprehensive approach seeks to provide valuable insights into PD progression and support the implementation of healthy habits in clinical practice.

Study Type

Observational

Enrollment (Estimated)

200

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

Patients diagnosed with Parkinson's disease

Description

Inclusion Criteria:

  • Patients with Parkinson's disease

Exclusion Criteria:

  • N/A

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Lifestyle intervention app
The group of patients includes individuals diagnosed with Parkinson's Disease (PD). This cohort encompasses a range of disease stages, severities, and demographic characteristics.
A technological smart platform (app) that integrates diets, physical activity programs, sleep habits and other lifestyle interventions

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Movement Disorder Society-Sponsored Revision of the Unified Parkinson's Disease Rating Scale (MDS-UPDRS)
Time Frame: From enrollment (app download) to 1 year
The MDS-UPDRS was developed to evaluate various aspects of Parkinson's disease including non-motor and motor experiences of daily living and motor complications. The MDS-UPDRS has a total score range of 0 to 236, with individual parts scoring between 0 to 52 (Parts I and II), 0 to 108 (Part III), and 0 to 24 (Part IV), assessing both motor and non-motor aspects of Parkinson's disease. A higher score indicates greater severity of Parkinson's disease symptoms.
From enrollment (app download) to 1 year

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Montreal Cognitive Assessment (MoCA)
Time Frame: At enrollment (app download) and after 1 year
The MoCA (Montreal Cognitive Assessment) scale has a total score range of 0 to 30, with higher scores indicating better cognitive function, and it assesses various cognitive domains such as memory, attention, language, and executive functions.
At enrollment (app download) and after 1 year

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Estimated)

September 1, 2026

Primary Completion (Estimated)

September 1, 2026

Study Completion (Estimated)

September 1, 2028

Study Registration Dates

First Submitted

December 23, 2024

First Submitted That Met QC Criteria

December 23, 2024

First Posted (Actual)

January 1, 2025

Study Record Updates

Last Update Posted (Actual)

December 1, 2025

Last Update Submitted That Met QC Criteria

November 27, 2025

Last Verified

November 1, 2025

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • TechHealthPD

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

UNDECIDED

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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