Interventional Study of the Effect of Parkinson Kinetigraph Recordings on the Clinical Management and Outcome in Parkinson's Disease
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 147
- 试验地点
- 2
- 主要终点
- Decision to change management
研究概览
简要总结
With time most people with Parkinson's disease (PwP) develop fluctuations in motor symptoms in relation to medication intake. The prevalence may be both under and overestimated as it is based on history rather than observation. Patterns in fluctuations are difficult to determine and it has been demonstrated that every 30-minute diaries need to be kept for 10 days or more to safely represent fluctuation patterns. The Parkinson Kinetigraph (PKG) is an automated system that is carried passively and provides similar information after wearing the device for 6 days. Clinical experience is that most patients agree that results are representative to their experiences. It is not known if using the PKG routinely at any stage of PD will change management of the disease. The hypothesis of this study is that providing PKG information to neurologists will lead to a more active management that may improve outcome in PD patients.
详细描述
Patients that have previously not performed a PKG recording will be recruited from the WestPORTS community based cohort of outpatients with PD in West Sweden. The WestPORTS study includes self-assessments like PDQ8 and NMS-Q as well as PKG recordings. On inclusion in WestPORTS-Int subjects will be randomized by minimization for age, gender and disease duration into one of two study arms. In the intervention group the PKG recording of the subject will be made available, together with a summarized interpretation, to the subject's regular neurologist/geriatrician before the next scheduled visit/contact. The neurologist will also be provided with PDQ8 and NMS-Q responses. In the control group only PDQ8 and NMS-Q responses will be available to the treating neurologist/geriatrician.
At the next regular visit/contact the physician will fill out an assessment of the state of the patient, whether stable or in need of change in management. Any contraindications to changed management will be noted and the decision to change or not change management will be recorded as the primary outcome of the study. Secondary outcomes are the patient reported experience of outpatient care according to a modified version of the Generic Short Patient Experiences Questionnaire (GS-PEQ), as well as patient reported (PDQ8, NMS-Q, PRO-PD, EQ5D5L) and PKG outcomes at a time point three months later.
Change of management is defined as any of the following:
- Adding or stopping a dopamine agonist, COMT- or MAO-inhibitor, anticholinergic or amantadine.
- Fractionation or de-fractionation of the current daily levodopa dose
- Change of current Levodopa Equivalent daily dose by 15% or more
- Start or stop of night medication
- Referral for device assisted therapy (LCIG, apomorphine pump or DBS)
Actual change of management (as opposed to decision to change) will be documented by retrospective review of medical records and prescription records. This will be a secondary measure.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- Double (Participant, Outcomes Assessor)
盲法说明
Patient not aware of which information has been provided to his/her physician. Post data collection the groups will be assigned coded group names so that the conditions are masked to the assessor.
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Clinical diagnosis of Parkinson's disease (ICD G209) according to medical records
- •A visit to an outpatient neurological or geriatric clinic in the region Vastra Gotaland, Sweden within the last -1 to -7 months according to medical records.
- •Randomized to invitation to participate in the WestPORTS objective measurement Cohort study (NCT03130595) by 1:4 randomization based on the full population fulfilling criteria 1 and
- •Written informed consent
- •No previous PKG recording has been performed with the subject.
排除标准
- •Withdrawal of consent.
- •Unable to wear a PKG on either wrist.
- •The patient's physician is the PI of the study (F Bergquist)
研究组 & 干预措施
Control
Treating physician will in advance of upcoming visit be provided with the self assessment scales PDQ8 and NMS-Questionnaire to aid clinical assessment
干预措施: Self assessment (Other)
Intervention
Treating physician will in advance of upcoming visit be provided with a Parkinson KinetiGraph recording report and interpretation in addition to the self assessment scales PDQ8 and NMS-Questionnaire to aid clinical assessment
干预措施: Parkinson KinetiGraph (Device)
Intervention
Treating physician will in advance of upcoming visit be provided with a Parkinson KinetiGraph recording report and interpretation in addition to the self assessment scales PDQ8 and NMS-Questionnaire to aid clinical assessment
干预措施: Self assessment (Other)
结局指标
主要结局
Decision to change management
时间窗: On first regular contact, RC, (telephone or visit) wich takes place within four months after PKG-recording
The decision to change management of Parkinson's disease as reported by the treating physician. Change of management is defined as any of the following: 1. Adding or stopping a dopamine agonist, COMT- or MAO-inhibitor, anticholinergic or amantadine. 2. Fractionation or de-fractionation of the current daily levodopa dose 3. Change of current Levodopa Equivalent daily dose by 15% or more 4. Start or stop of night medication 5. Referral for device assisted therapy (LCIG, apomorphine pump or DBS)
次要结局
- Parkinson Kinetigraph bradykinesia measurement at 3 months after the first regular visit(The assessment is made 3 months after the RC.)
- Actual change of management(Change should take place within 4 weeks from the RC.)
- PRO-PD score at 3 months after the first regular visit(The assessment is made 3 months after the RC.)
- Parkinson Kinetigraph dyskinesia measurement at 3 months after the first regular visit(The assessment is made 3 months after the RC.)
- NMSQ score at 3 months after the first regular visit(The assessment is made 3 months after the RC.)
- EQ5D-5L at 3 months after the first regular visit(The assessment is made 3 months after the RC.)
- Change in NMSQ compared to baseline(Assessed 3 months after the RC and at end of study 12 months after inclusion visit)
- Change in EQ5D5L compared to baseline(Assessed 3 months after the RC and at end of study 12 months after inclusion visit)
- Change in Parkinson Kinetigraph fluctuation score compared to baseline(Assessed 3 months after the RC and at end of study 12 months after inclusion visit)
- Patient Reported Experience of Care(The assessment will be made within 3 days from the first RC after PKG-recording,)
- PDQ-8 score at 3 months after the first regular visit(The assessment is made 3 months after the RC.)
- Change in PDQ8 compared to baseline(Assessed 3 months after the RC and at end of study 12 months after inclusion visit)
- Parkinson Kinetigraph fluctuation score at 3 months after the first regular visit(The assessment is made 3 months after the RC.)
- Parkinson Kinetigraph Tremor measurement at 3 months after the first regular visit(The assessment is made 3 months after the RC.)
- Parkinson Kinetigraph immobility measurement at 3 months after the first regular visit(The assessment is made 3 months after the RC.)
- Change in Parkinson Kinetigraph bradykinesia score compared to baseline(Assessed 3 months after the RC and at end of study 12 months after inclusion visit)
- Change in Parkinson Kinetigraph Immobility measurement compared to baseline(Assessed 3 months after the RC and at end of study 12 months after inclusion visit)
- Change in Parkinson Kinetigraph dyskinesia score compared to baseline(Assessed 3 months after the RC and at end of study 12 months after inclusion visit)
- Change in Parkinson Kinetigraph Tremor measurement compared to baseline(Assessed 3 months after the RC and at end of study 12 months after inclusion visit)
研究者
Filip Bergquist
Associate Professor
Sahlgrenska University Hospital, Sweden