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CHIEF-PD (CHolinesterase Inhibitor to prEvent Falls in Parkinson's Disease)

CHolinesterase Inhibitor to prEvent Falls in Parkinson's Disease: A Phase 3 Randomised, Double-blind Placebo-controlled Trial of Rivastigmine to Prevent Falls in Parkinson's Disease.

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04226248
Acronym
CHIEF-PD
Enrollment
600
Registered
2020-01-13
Start date
2020-01-02
Completion date
2025-07-24
Last updated
2025-09-29

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

Conditions

Parkinson Disease

Keywords

Parkinson Disease, Parkinson, Rivastigmine, Falls, Cholinesterase Inhibitors, Phase III

Brief summary

Parkinson's disease is a common condition particularly affecting older people. Falls are a very frequent complication of the disease affecting 60% of people with Parkinson's every year. As the population ages, the number of people living with Parkinson's disease and the occurrence of complications will increase. The loss of the chemical dopamine in the brain causes walking in Parkinson's to become slower, unsteady and irregular. People with the condition are therefore at a very high risk of falling. To some extent, people can compensate for these changes by paying more attention to their walking. However, Parkinson's also diminishes memory and thinking ability. This decreases people's ability to pay attention to their walking, especially when doing something at the same time. Cholinesterase inhibitor (ChEis) are drugs that are currently used to treat people with memory problems in Parkinson's. The effect of these drugs on falls in Parkinson's has been tested to show that treatment has the potential to almost halve the number of falls. This trial aims to definitively determine whether cholinesterase inhibitors (ChEi), can prevent falls in Parkinson's and whether this treatment is cost effective. 600 participants with Parkinson's disease will be enrolled from hospitals throughout the UK. Participants will be randomly assigned to either receive the drug (ChEi) via a patch or receive a placebo (dummy) treatment via a patch. Neither the researchers nor the participants will know which group they are in. Participants will take the medication for 12 months and record any falls that they experience in diaries. If successful, this treatment in Parkinson's disease, would tackle one of the most disabling complications of the disease and positive findings will provide robust evidence to change clinical practice.

Interventions

Rivastigmine Trandermal Patches applied once a day for up to 12 months

OTHERPlacebo Transdermal System

Placebo Trandermal Patches applied once a day for up to 12 months

Sponsors

Royal United Hospitals Bath NHS Foundation Trust
CollaboratorOTHER
University of Bristol
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Masking description

Double blind

Intervention model description

A Phase III Randomised Controlled Trial of Rivastigmine versus Placebo

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Diagnosis of idiopathic Parkinson's disease. * Modified Hoehn and Yahr stage 1-4 disease as determined at baseline visit. * Have experienced a fall in the previous year. * Able to walk ≥10m without aids or assistance. * 18+ years of age.

Exclusion criteria

* Previous ChEi use in 12 months prior to enrolment. * Hypersensitivity to rivastigmine * Dementia diagnosed according to MDS criteria (6). * Inability to attend or comply with treatment or follow-up scheduling. * Non-English-speaking patients (cognitive tests performed in English). * Falling ≥4x per day. * Unwillingness to use an acceptable method of contraception for the duration of the trial if they are of childbearing potential. * Pregnancy and/or breastfeeding

Design outcomes

Primary

MeasureTime frameDescription
Fall rate12 months from the day the IMP is commencedFall rate measured using monthly diaries and telephone calls prospectively

Secondary

MeasureTime frameDescription
Parkinson's Disease (PD)12 monthsMDS-UPDRS total score in the practically defined 'ON' state and each individual subscale (1-4)
Freezing of gait12 monthsNew Freezing of Gait Questionnaire (NFOGQ)
Frailty12 monthsFrailty assessed by the SHARE-FI
Physical performance12 monthsMeasured by the Short physical performance battery (SPPB)
Freezing of Gait Assessment12 monthsGait speed measured with Freezing of Gait (turn test)
Gait Assessment12 monthsGait speed measured with and without dual task
Cognition12 monthsMontreal Cognitive Assessment (MoCA)
Dysphagia12 monthsSwallowing Disturbance Questionnaire (SDQ)
Fear of falling12 monthsIconographical Fall Efficacy Scale (ICON-FES)
Participant health related quality of life0,1,3,6 9 and 12 monthsEuroQoL 5D-5L health status questionnaire (EQ-5D-5L)
Capability of older people12 monthsICEpop CAPability measure for Older people (ICECAP-O)
Mortality (all cause and PD-related)12 monthsOffice of National Statistics (ONS) data
Cost effectiveness by NHS resource use12 monthsNHS Hospital Episode Statistics (HES) data
Apathy12 monthsStarkstein Apathy Scale
Depression12 monthsGeriatric Depression Scale (GDS)

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 20, 2026