Walking Pattern Characteristics in Normal Pressure Hydrocephalus

Idiopathic Normal Pressure Hydrocephalus (INPH) Clinical Trial

— NPH wearables  

Official title:

Walking Pattern Characteristics in Normal Pressure Hydrocephalus. A Phase I/II Open-label Single Center Trial to Characterize Disease-specific Walking Patterns Using Wearable Gyroscopes

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04702035
• Other study ID #: NPH wearables
• Status: Completed
• Phase: N/A
• Start date: January 1, 2018
• Est. completion date: April 25, 2024

Study information

• Verified date: April 2024
• Source: University of Zurich
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

20 patients who are diagnosed with NPH receive a set of 5 wearable gyroscopes (IMUs, ZurichMove sensors) for a period of 3 days for measurement and characterization of their walking in an ambulatory setting. At a follow-up 2 weeks to 6 months after CSF diversion surgery, the examination is repeated and improvement is measured. The data will be compared with a healthy group of 20 age- and gender-matched individuals as well a a group of 20 young individuals.

Description:

Temporary attachment of IMUs to wrists and ankles of the patients and probands for a period of three days and recording of movement during a 10 meter-walking test, 180° turnaround and during normal movement at home.

Group 1 (patients):

Patients with a completed diagnostic concerning iNPH, who are planned to receive a VP-shunt by their responsible neurosurgeon (independently from the study), will be included.

Before the shunt implantation, the patients will be examined at the USZ using wearable gyroscopes (like wristwatches) at both wrists and ankles as well as one around the body center.

The short examination will comprise a patient history (MoCa test, Kiefer-score, Stein- and Langfitt-Score), a short examination (4 minute walking test, 180° turnaround) in hospital. Afterwards, the patient goes home, where the gyroscopes examine walking patterns for a period of three days. After this period, the patient brings the devices back to the hospital. The surgery will take place afterwards, independently from the study, as well as adjustments of the shunt's flow-resistance for achievement of optimal response to the therapy. After this optimal result is achieved, but latest after 6 months, the examination will be repeated.

Groups 2 and 3 (controls):

As well 20 subjects matched for sex and age with the patient's group as 20 healthy young subjects will be examined just like the patients preoperatively. Walking patterns shall be compared to identify changes between pre- and postoperatively as well as differences between patients and controls.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 60
• Est. completion date: April 25, 2024
• Est. primary completion date: April 25, 2024
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 100 Years

Eligibility

Age limits for the NPH patient group and the matched healthy vonunteers group are 60-100 years.

Age limits for the young healthy volunteers group are 18-40 years.

Inclusion Criteria:

NPH patient group:

1. Informed Consent as documented by signature prior to any study related procedures or informed consent by a legal representative in case of cognitive deficits.

2. Male and female patients alike

3. Age between 60 and 100 years

4. Clinical suspect for NPH

5. Significant improvement (by more than 10%) in walking speed or endurance in a standardized CSF-TAP test (of at least 35 ml CSF).

6. Planned implantation of a VP shunt for NPH treatment (independently from the study).

Matched controls group:

1. Informed Consent as documented by signature prior to any study related procedures

2. Male and female patients alike (matched to group 1)

3. Age between 60 and 100 years (matched to group 1)

4. No clinical suspect for NPH or any other movement disorder

Young controls group:

1. Informed Consent as documented by signature prior to any study related procedures

2. Male and female patients alike (matched to group 1)

3. Age between 18 and 40 years

4. No clinical suspect for NPH or any other movement disorder

Exclusion Criteria:

1. Enrolment of the investigator, his/her family members, employees and other dependent persons (only for patients; no exclusion criteria for controls),

2. Apparent or suspected movement disorder or other known disorder, which might affect normal standing or walking

3. Cardiovascular disorders, which might affect physical resilience

4. Pregnant women

5. Pre-menopausal state of female patients and probands in groups 1 and 2.

6. Children and adolescents

Related Conditions & MeSH terms

• Hydrocephalus
• Hydrocephalus, Normal Pressure
• Idiopathic Normal Pressure Hydrocephalus (INPH)

Intervention

Device:
• Characterization of walking pattern characteristics in an ambulatory setting using wearable IMUs (ZurichMOVE sensors)
All participants receive a set of 5 wearable IMUs for a period of 3 days. The IMUs are fixed at both wrists, ankles and one over the sternum. A 10-meter walking test, 180 degree turnaround test and normal walking at home are performed. Afterwards, the IMUs are removed for data extraction and evaluation. The patient group is examined a second time after CSF diversion surgery.

Locations

Country	Name	City	State
Switzerland	Dept. of Neurosurgery, Zurich University Hospital	Zurich

Sponsors (2)

Lead Sponsor	Collaborator
University of Zurich	ETH Zurich

Country where clinical trial is conducted

Switzerland, 

References & Publications (1)

Renggli D, Graf C, Tachatos N, Singh N, Meboldt M, Taylor WR, Stieglitz L, Schmid Daners M. Wearable Inertial Measurement Units for Assessing Gait in Real-World Environments. Front Physiol. 2020 Feb 20;11:90. doi: 10.3389/fphys.2020.00090. eCollection 2020. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Walking characteristics	Complex walking pattern comprising of stride length, width, frequency (altogether one parameter)	Between 2 weeks to 6 months after CSF diversion surgery
Secondary	4 minutes timed Walk test	Standard test (seconds)	immediately after fixation of IMUs
Secondary	180 degree turnaround test	Participants are asked to turn by 180 degrees. Steps needed are counted.	immediately after fixation of IMUs
Secondary	Kiefer score	Standard score for iNPH severity, only patient group; range 0-26; higher indicates higher severity	before surgery
Secondary	Kiefer score	Standard score for iNPH severity, only patient group; range 0-26; higher indicates higher severity	after surgery (range 2 weeks to 6 months)
Secondary	Stein and Langfitt score	Standard score for patient independence, only patient group; range 0-IV; higher indicates higher dependency	before surgery
Secondary	Stein and Langfitt score	Standard score for patient independence, only patient group; range 0-IV; higher indicates higher dependency	after surgery (range 2 weeks to 6 months)
Secondary	NPH recovery rate	Standard rate for success of CSF diversion treatment in NPH. Calculated as follows: (Kiefer score preoperatively - Kiefer score postoperatively) / Kiefer score preoperatively x 10; range 0-10; Higher indicates better response to surgery	after surgery (range 2 weeks to 6 months)
Secondary	Evan´s Index	Standard descriptor for width of lateral ventricles in iNPH. Calculated as maximum with of frontal horns / maximal diameter of brain in axial CT or MRI at the level of cella media; range: 0-1; higher indicates larger ventricles and more severe hydrocephlaus	before surgery
Secondary	Disproportionally Enlarged Subarachnoidal space Hydrocephalus (DESH) sign	Positivity of standard sign in preoperative CT or MRI imaging, hinting at presence of iNPH. Values: Positive/Negative	before surgery
Secondary	Time from appearance of first symptoms to surgery	From first appearance of symptoms to surgery in years	before surgery
Secondary	3-dimensional characterization of walking patterns	Detailed analysis of walking patterns recorded during the measurement phases by the wearable IMUs.	before surgery
Secondary	3-dimensional characterization of walking patterns	Detailed analysis of walking patterns recorded during the measurement phases by the wearable IMUs.	after surgery (range 2 weeks to 6 months)