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Evaluation of a proactive approach to health care in Parkinson's disease: a randomized controlled trial

Evaluation of a proactive approach to health care in Parkinson's disease: a randomized controlled trial - ParkProReakt

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00031092
Enrollment
292
Registered
2023-06-29
Start date
2024-01-01
Completion date
Unknown
Last updated
2025-11-24

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

Conditions

G20

Interventions

Group 1: Care according to the ParkProReakt model in addition to regular health care Group 2: Regular health care (no intervention)

Sponsors

Philipps Universität Marburg - Klinik für Neurologie
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. patients (m/f/d) with a clinical diagnosis of Idiopathic Parkinson's Syndrome (IPS). 2. severity Hoehn & Yahr stage I-IV 3. at least 18 years old 4. good knowledge of German 5. able and willing to give consent 6. able to remember information, use it to make a decision, and communicate decisions through speech, sign language, or other means

Exclusion criteria

Exclusion criteria: 1. other diseases affecting cognition are present (e.g. tumors etc.) 2. refusal or inability to participate in the study 3. other comprehension and communication difficulties that interfere with inclusion criteria (e.g., language problems)

Design outcomes

Primary

MeasureTime frame
The primary outcome of the study is health-related quality of life measured by the 39-item Parkinson's Disease Questionnaire (PDQ-39). The primary outcome will be examined at the following time points: baseline (t0), monthly (t1-5) and after 6 months (t6). Peto, V., Jenkinson, C., & Fitzpatrick, R. (1998). PDQ-39: a review of the development, validation and application of a Parkinson's disease quality of life questionnaire and its associated measures. Journal of neurology, 245 Suppl 1, S10–S14. https://doi.org/10.1007/pl00007730

Secondary

MeasureTime frame
Subjective well-being of patients, onset or change in care needs, global cognition/disease progression, utilization of healthcare services and frequency of hospital stays, burden on family caregivers.

Countries

Germany

Contacts

Public ContactDavid Pedrosa

Philipps Universität Marburg

david.pedrosa@staff.uni-marburg.de+4964215865299

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 5, 2026