Adapted Physical Activity and Tango-Based Therapy for Parkinson's Disease: A Pilot Study
NCT07736014
Basal Ganglia Diseases, Brain Diseases
Foggia, FG, Italy
View Trial DetailsNCT Number: NCT02381444
The aim of this study is to assess the effect of LCIG (levodopa-carbidopa intestinal gel) on HRQL (Health-Related Quality of Life) of participants and compare the Health-Related Quality of Life between participants continuing to levodopa-carbidopa intestinal gel treatments versus participants continuing on oral therapy for Parkinson's Disease.
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Notify Me18 year–99 year
All sexes
Observational
Universitaetsklinikum Aachen /ID# 204355, Aachen, North Rhine-Westphalia, Germany
Parkinson's disease (PD) is the second most common neurodegenerative disorder in the world. It can be treated sufficiently until motor complications with fluctuations of mobility and dyskinesia develop. The quality of life is relentlessly deteriorating with longer disease duration once the complications of conservative oral therapy develop. Continuous dopaminergic stimulation using Levodopa/Carbidopa Intestinal Gel (LCIG) improves the motor complications of Parkinson's disease and preliminary data suggest that also the quality of life is improved. Primary Objective is to assess the effect of LCIG on Health Related Quality of Life (HRQL) of patients according to selection criteria from German guidelines and compare improvement in HRQL between patients continuing to LCIG treatment and patients staying on oral treatment, despite being eligible according to these guidelines. In addition, current selection criteria recommended by the national guideline will be documented at baseline.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: From baseline to 12 months
The primary endpoint is the change in the Parkinson's Disease Questionnaire (PDQ-39) summary index from 12 months to the baseline assessment. The two treatment groups levodopa-carbidopa intestinal gel vs. Standard of Care will be compared.
Time frame: At Baseline, 6, and 12 months of treatment
Unified Parkinson's disease Rating Scale (UPDRS) part III in the medication "on" state
Time frame: From Baseline to 6 and 12 months of treatment.
Activities of daily living "on" and "off" medication - Unified Parkinson's disease Rating Scale (UPDRS) part II
Time frame: From Baseline to 6 and 12 months of treatment
Frequency and severity of ON-dyskinesia (Unified Parkinson's Disease Rating Scale part IV, Complications of Therapy: Items 32, 33, 34 and 39)
Time frame: From baseline to 6 and 12 months of treatment
Non Motor Symptoms Scale (NMSS) Total score and subdomains Cardiovascular, Sleep/Fatigue, Gastrointestinal, Urinary, Sexual functioning
Time frame: At Baseline, 6 and 12 month
There are no data comparing long-term HRQL of LCIG versus peroral therapy
Time frame: From Baseline to 6 and 12 months of treatment
Non Motor Symptoms Scale (NMSS) Total score and subdomains Cardiovascular, Sleep/Fatigue, Gastrointestinal, Urinary, Sexual functioning
AbbVie
Industry
Health Related Quality of Life in LCIG Patients and LCIG Patients and LCIG Eligible Patients Continuing Oral Therapy. A Multicenter Post Marketing Observational Study for LCIG in Germany and Switzerland - BALANCE
Acronym: BALANCE
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