NCT Number: NCT00349310
Profile of Depressive Symptoms in Parkinsons Disease
To explore or establish the relationship between cognitive, mood and motor symptoms in PD to scores on depression rating scales in a naturalistic setting.
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Notify MeKey information
Conditions
Age range
18 year and older
Sex eligibility
All sexes
Study type
Observational
Primary location
Boehringer Ingelheim Investigational Site, Innsbruck, Austria
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion_Criteria:
Observation criteria:
- are able to provide written informed consent in accordance with Good Clinical Practice (GCP) and local legislation
- have idiopathic Parkinsons disease according to the United Kingdom Parkinsons Disease Society Brain Bank Diagnostic Criteria for Parkinsons disease
- show no impairment of cognitive function (MMSE score ?24)
- are with or without symptoms of depression (full range)
- are stable on anti-Parkinson/anti-depressive treatment for at least 1 month before entering the study
- are or are not on concomitant antidepressant treatment
- are in the on state during the observation period
- did not previously undergo PD surgery
Treatment and study plan
Primary outcomes
-
HADS, HAMD-17, BDI-1A, FAB (cognitive), DSM-IV (mood- part A, B, C, E) and UPDRS
Time frame: Up to 6 months
Sponsors and collaborators
Lead sponsor
Boehringer Ingelheim
Industry
Registry information
Official study title
Profile of Depressive Symptoms in Parkinson's Disease (PRODEST-PD)
Important dates
- Study start
- 2006
- Primary completion
- 2006
- Study completion
- 2006
- First posted
- Jul 6, 2006
- Registry last updated
- Dec 14, 2023
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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