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Integrated Multidisciplinary Care for Parkinson's Disease: a Controlled Trial

Integrated Multidisciplinary Care for Parkinson's Disease: a Controlled Trial

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00518791
Enrollment
301
Registered
2007-08-21
Start date
2007-08-31
Completion date
2010-08-31
Last updated
2010-11-05

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

Conditions

Parkinson's Disease

Keywords

Integrated health care system, Treatment effectiveness, Cost effectiveness, Program evaluation

Brief summary

The aim of the present study is to evaluate the (cost) effectiveness of a new health care system in which an individualised multidisciplinary assessment is given to patients with Parkinson's Disease(PD)in combination with treatment by a dedicated team of specifically trained health professionals, compared to usual care. Overall, we anticipate to gain more insight in the clinical effectiveness and health care costs of multidisciplinary treatment in PD.

Detailed description

PD is a complex disorder, with motor as well as non-motor symptoms. Despite the complexity of PD, management of the disease is often 'monodisciplinary' since most patients are only treated by a neurologist. Stimulating compensatory strategies by allied health professionals might offer additional therapeutic relief, but this assumption is mainly based on theoretical arguments and expert opinion. Even less is known about the claim that a multidisciplinary team of multiple professionals active in complementary domains (e.g. physiotherapy, occupational therapy and speech therapy) is superior to management by each of these professionals alone. This study anticipates to provide more insight in the clinical effectiveness and health care costs of multidisciplinary treatment in PD. Therefore, our multidisciplinary care concept (a comprehensive assessment by a dedicated multidisciplinary team and subsequent treatment by specifically trained health professionals) that is tailored to the patients' individual needs will be compared to usual care in terms of effectiveness and costs.

Interventions

A comprehensive individualised assessment by a dedicated multidisciplinary team (Multidisciplinary Assessment Center) and subsequent treatment by specifically trained health professionals (ParkinsonNet).

OTHERUsual Care

No altered organisation of care

Sponsors

Stichting Nuts Ohra
CollaboratorOTHER
Porticus
CollaboratorUNKNOWN
Radboud University Medical Center
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
20 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* Patients with Idiopathic PD, diagnosed according to the Brain Bank Criteria of the UK Parkinson's Disease Society * Regular control by the neurologist * Living independently in the community * Able to complete the trial questionnaires

Exclusion criteria

* Atypical parkinsonian syndromes * Hoehn and Yahr stage 5 * Severe cognitive impairment (MMSE\<24) * Presence of other neurological disorders * Severe co-morbidity (e.g. cancer) * Planned surgical procedure for PD within the intervention period * Patients who have already visited the Multidisciplinary Assessment Center

Design outcomes

Primary

MeasureTime frame
Parkinson's Disease Quality of Life Questionnaire (PDQL)8 months
AMC Linear Disability Score (ALDS)8 months

Secondary

MeasureTime frame
UPDRS Complications of therapy (part IV)(tertiary)4 months
SPDDS(tertiary)8 months
Modified MACTAR scale(tertiary)8 months
Parkinson Activity Scale(tertiary)4 months
Costs (secondary)8 months
SF-36 (secundary;utility score)8 months
Freezing of Gait Questionnaire (tertiary)8 months
Falls Efficacy Scale (tertiary)8 months
Non-Motor Symptom Assessment Scale and Quest for Parkinson's Disease (tertiary)8 months (Quest) and 4 months (Scale)
Hospital Anxiety and Depression Scale (tertiary)8 months
Caregiver burden assessed with BELA-A-k (secondary), SF-36 (tertiary), and HADS (tertiary)8 months
Frequency of falls (tertiary)8 months
UPDRS Motor Examination (part III)(secondary)4 months

Countries

Netherlands

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 22, 2026