DetectFoG : Detection of Gait Freezing Episodes in Parkinsonian Patients Using Inertial Measurement Units

NCT ID: NCT05822258

Last Updated: 2024-10-09

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

20 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-01-08

Study Completion Date

2026-08-08

Brief Summary

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Parkinson's disease is the second most common neurodegenerative disease in the world. One of these manifestations is the freezing of gait (FOG) which affects 50 to 80% of Parkinsonian patients. It is defined as a brief and episodic absence or marked reduction in the forward progression of the feet despite the intention to walk. FOG is one of the most disabling symptoms causing a greater risk of falling and a loss of autonomy for these patients. This symptom is little or not dopamine-sensitive and little improved by surgery (deep brain stimulation).

Although this symptom is common and debilitating, it is difficult to assess clinically. The objective assessment of the presence and severity of FOG episodes can be done with tests such as the New-Freezing of Gait Questionnaire (N-FOGQ) with however limitations. Indeed, this filmed examination is scored a posteriori and the accumulation of the administration times which makes it difficult to use in routine clinical practice. To overcome these limitations, the use of a diary completed by the patient himself is a simple alternative to assess this symptom, but studies show that patients abandon this practice in the long term and that it is not used by patients with cognitive impairment.

Recent advances in miniaturization have made it possible to create light and compact sensors to assess these events objectively. Inertial measurement units have been widely used in the literature to detect FOG episodes. The choice of the detection algorithms are a major issue in the scientific community. To date, due to the heterogeneity of the protocols, no method is currently required as a reference.

The objective is to evaluate the accuracy of a new algorithm to detect the number of FOG episodes in Parkinsonian patients. This evaluation will be done on the freeze-inducing walking path.

Detailed Description

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Conditions

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Parkinson Disease

Study Design

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Allocation Method

NA

Intervention Model

SEQUENTIAL

Patients will be evaluated in the "ON" state phase and in the "OFF" state phase.

For each visit, the patient will be asked to walk at a comfortable speed under the following 3 conditions: motor task, verbal, normal.
Primary Study Purpose

DIAGNOSTIC

Blinding Strategy

NONE

Study Groups

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Freezing of Gait

Each patient will have 2 visits :

* First visit in the "ON" state phase, i.e. when their oral treatment allows the maximum improvement of dopamine-responsive parkinsonian symptoms.
* A second visit in the "OFF" phase after having stopped taking their antiparkinsonian medications for at least 12 hours before the start of the visit, in order to promote episodes of FOG

For each visit, the patient will be asked to walk at a comfortable speed under the following 3 conditions:

* Normal condition without additional physical and verbal tasks
* Condition with added physical tasks: The physical task of holding a ball in the center of a tray.
* Condition with added verbal tasks: The verbal task of saying as many words as possible starting with a specific letter.

Conditions of passage are randomized per patient. Each subject will complete the course a maximum of 18 times in blocks of 3 conditions (normal, double physical task and double verbal task). A rest period will be observed.

Group Type EXPERIMENTAL

Walk under 3 conditions (normal, physical tasks, verbal tasks)

Intervention Type OTHER

Each patient will have 2 visits :

* First visit in the "ON" state phase, i.e. when their oral treatment allows the maximum improvement of dopamine-responsive parkinsonian symptoms.
* A second visit will be scheduled 15 +/- 7 days from the first. Patients will then be assessed in the "OFF" phase after having stopped taking their antiparkinsonian medications for at least 12 hours before the start of the visit, in order to promote episodes of FOG

For each visit, the patient will be asked to walk at a comfortable speed under the following 3 conditions:

* Normal condition without addition of additional physical and verbal tasks
* Condition with added physical tasks: The physical task of holding a ball in the center of a tray
* Condition with added verbal tasks: The verbal task of saying as many words as possible starting with a specific letter.

Conditions of passage are randomized per patient. Each subject will complete the course a maximum of 18 times in blocks of 3 conditions.

Interventions

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Walk under 3 conditions (normal, physical tasks, verbal tasks)

Each patient will have 2 visits :

* First visit in the "ON" state phase, i.e. when their oral treatment allows the maximum improvement of dopamine-responsive parkinsonian symptoms.
* A second visit will be scheduled 15 +/- 7 days from the first. Patients will then be assessed in the "OFF" phase after having stopped taking their antiparkinsonian medications for at least 12 hours before the start of the visit, in order to promote episodes of FOG

For each visit, the patient will be asked to walk at a comfortable speed under the following 3 conditions:

* Normal condition without addition of additional physical and verbal tasks
* Condition with added physical tasks: The physical task of holding a ball in the center of a tray
* Condition with added verbal tasks: The verbal task of saying as many words as possible starting with a specific letter.

Conditions of passage are randomized per patient. Each subject will complete the course a maximum of 18 times in blocks of 3 conditions.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* Patient over 18 years old
* With Parkinson's disease according to the United Kingdom Brain Bank criteria
* Presenting episodes of freezing of gait assessed on the Movement Disorder Society-Unified Parkinson's Disease Rating Scale (MDS-UPDRS II - question 13 with a score between 1 and 3 in order to have a patient walking without technical assistance) produced by the neurologist
* Able to walk 30 meters independently
* Affiliated to a social security scheme or beneficiary of such a scheme
* Having signed a free and informed consent in writing

Exclusion Criteria

* Montreal Cognitive Assessment (MOCA) \< 20/30
* Other neurological or orthopedic history that interferes with walking
* Pregnant, parturient or breastfeeding women
* Adults subject to legal protection (safeguard of justice, curatorship, guardianship), persons deprived of liberty
* Persons undergoing psychiatric care, persons admitted to a health or social establishment for purposes other than research
* Minors
* Persons unable to express their consent
* Simultaneous participation in another research related to balance and/or walking
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Rennes University Hospital

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Rennes University Hospital

Rennes, Brittany Region, France

Site Status RECRUITING

Countries

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France

Facility Contacts

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Karim Jamal, MD

Role: primary

02 99 28 90 51 ext. 0033

[email protected], MD

Role: backup

References

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Cordillet S, Drapier S, Leh F, Dumont A, Bidet F, Bonan I, Jamal K. Detecting Freezing of Gait in Parkinson Disease Using Multiple Wearable Sensors Sets During Various Walking Tasks Relative to Medication Conditions (DetectFoG): Protocol for a Prospective Cohort Study. JMIR Res Protoc. 2025 Feb 6;14:e58612. doi: 10.2196/58612.

Reference Type DERIVED
PMID: 39913915 (View on PubMed)

Other Identifiers

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2023-A00561-44

Identifier Type: OTHER

Identifier Source: secondary_id

23.01067.000298

Identifier Type: OTHER

Identifier Source: secondary_id

35RC22_9907-12_DetectFoG

Identifier Type: -

Identifier Source: org_study_id

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