Parkinson Disease Clinical Trial
— PROUDOfficial title:
A Model of Hospital-territory Management Coordinated by a Case Manager to Improve the Care of Patients With Parkinsonism. A Multicenter, Randomized, Double-blind Study. The PROUD Study
Verified date | March 2024 |
Source | Fondazione I.R.C.C.S. Istituto Neurologico Carlo Besta |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The present multicenter randomized study investigates whether the management of patients with parkinsonism by a nurse specialist (case-manager) can significantly improve patients' quality of life over 12 months, compared to control patients managed with the standard-of-care process. Participants will be evaluated with clinical scales testing quality of life, motor and non-motor symptoms, and the number of unscheduled hospital access throughout the course of the study.
Status | Active, not recruiting |
Enrollment | 121 |
Est. completion date | June 30, 2025 |
Est. primary completion date | January 30, 2025 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Age = 18 years - Living in the Lombardy region (Northern Italy) - Duration of Parkinson's disease, atypical or secondary parkinsonism = 3 years - Presence of at least (i) n=1 motor complication and/or (ii), n=2 non-motor symptoms, defined as follows: (i) Motor complication: - Motor fluctuations - = 2 Falls in the last 6 months - Dysphagia (ii) Non Motor symptoms - Non-motor fluctuations - = 2 items of the non-motor symptoms scale with a score = 2 Exclusion Criteria: - Hoehn and Yahr Stage = 5 in the ON-medication condition - Psychiatric comorbidity or other neurological chronic diseases that, in the opinion of the recruiting neurologist, could compromise the study participation. - Patients on infusional therapies (continuous infusion of levodopa-carbidopa intestinal gel or Continuous Subcutaneous Apomorphine Infusion). - Severe medical disease (liver or kidney failure, decompensated heart disease, neoplasms, coagulopathy) |
Country | Name | City | State |
---|---|---|---|
Italy | Fondazione IRCCS Istituto Neurologico Carlo Besta | Milan | |
Italy | Azienda Socio-Sanitaria Territoriale Nord Milano | Sesto San Giovanni | Milan |
Lead Sponsor | Collaborator |
---|---|
Fondazione I.R.C.C.S. Istituto Neurologico Carlo Besta | Azienda Socio Sanitaria Territoriale Nord Milano |
Italy,
Bloem BR, Henderson EJ, Dorsey ER, Okun MS, Okubadejo N, Chan P, Andrejack J, Darweesh SKL, Munneke M. Integrated and patient-centred management of Parkinson's disease: a network model for reshaping chronic neurological care. Lancet Neurol. 2020 Jul;19(7):623-634. doi: 10.1016/S1474-4422(20)30064-8. Epub 2020 May 25. — View Citation
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* Note: There are 16 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Changes in total score of the Parkinson's Disease Questionnaire 39-items scale | Thi is a 39-items questionnaire assessing the quality of life of patient with Parkinson's disease. The higher the score the lower the quality of life | baseline, week 52 | |
Secondary | Number of unscheduled hospital access over the 12-month study period | The investigators will collect the sum of the number of (i) extra unscheduled outpatient visits, (ii) emergency room visits, (iii) hospital admissions directly or indirectly associated with parkinsonism | baseline, week 26, week 52 | |
Secondary | Changes in the Movement Disorder Society Unified Parkinson's Disease Rating Scale part II | This is a scale (MDS-UPDRS) used to assess activities of daily living. The higher the score the worse the Disability | baseline, week 52 | |
Secondary | Changes in the Movement Disorder Society Unified Parkinson's Disease Rating Scale part IV | This is a scale (MDS-UPDRS) used to assess complications of dopaminergic therapy. The higher the score the worse the disability | baseline, week 52 | |
Secondary | Changes in the Non-Motor Symptoms Scale score | This is a scale used to assess the burden of non-motor symptoms in Parkinson's disease. The higher the score the worse the disability | baseline, week 52 | |
Secondary | Changes in the activities of daily living questionnaire | The "ADL (Activities of Daily Living)" evaluation refers to the fundamental activities of daily life in which the subject is dependent: on a scale from 0 to 6 points, the lower the score, the greater the person's need for assistance | baseline, week 52 | |
Secondary | Changes in the instrumental activities of daily living questionnaire | The "IADL (Instrumental Activities of Daily Living)" evaluation refers to the instrumental activities of daily life in which the subject is dependent (eg using telephone, preparing meals, taking medications, etc): on a scale from 0 to 8 points, the lower the score, the greater the person's need for assistance | baseline, week 52 | |
Secondary | Changes in patient experience questionnaire | This is a questionnaire assessing patient perception and satisfaction of the quality of health care | baseline, week 26, week 52 | |
Secondary | Changes in EuroQOL-5 Dimensions-5 Levels score | This is a useful and validated instrument to measure quality of life in patients with Parkinson's disease | baseline, week 52 | |
Secondary | Changes in the Morisky Medical Adherence scale-8 items score | This is an 8-items scale used to investigate patient adherence to the therapy prescribed by the MD specialist | baseline, week 26, week 52 | |
Secondary | Changes in the Zarit Burden Interview scale score | This is a scale used to investigate caregiver's burnout | baseline, week 26, week 52 | |
Secondary | Number of incident comorbidities | The number of incident comorbidities over the 12.month study period will be assessed using a semistructured interview | baseline, week 26, week 52 |
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