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Improving Posture in Parkinson's Patients Through Home-based Training and Biofeedback

Improving Posture in Parkinson's Patients Through Home-based Training and Biofeedback

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03477695
Enrollment
60
Registered
2018-03-26
Start date
2018-04-01
Completion date
2019-12-31
Last updated
2018-05-08

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

Conditions

Parkinson's Disease and Parkinsonism, Postural Kyphosis

Brief summary

A stooped posture is one of the characteristic motor symptoms of patients with Parkinson's disease, and has been linked to impairments in ADL and QOL. We aimed to test the efficacy, safety, practical utility and user-friendliness of a posture correction and vibrotactile trunk angle feedback device (the UpRight) in the home setting of patients with Parkinson's disease with a stooped posture.

Detailed description

The subjects will be asked to arrive at the Gait laboratory for Mobility Research at Tel Aviv Medical Center. After a detailed explanation of the research procedure and after signing the consent form, they will be introduced to the UPRIGHT GO device. Participances will practice operating and placing the device on the body. With the device attached to upper back, a number of short clinical tests will be performed: 1. Complete demographic questionnaires and medical history 2. Walking tests and balance: 1. Short walks at a comfortable speed with or without dual task. 2. Stairs 3. Performing daily tasks, such as entering and exiting a room, negotiating obstacles (shoebox), walking between obstacles, buttons, tying laces, carrying small objects on a tray, bringing a glass of water etc. 4. Timed Get up and go test All tests are supervised by a physiotherapist . Upon completion of the tests, the UPRIGHT device will be delivered for use and exercise for 2 months. Physiotherapist will guide to maintain the devices (such as charging devices and connecting to power). At the end of the training period, the participans will be invited again to Gait Lab for post tests.

Interventions

DEVICEambulatory use of the Upright device

Patients will wear the UpRight for a period of two month

Sponsors

Tel-Aviv Sourasky Medical Center
Lead SponsorOTHER_GOV

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
50 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

1. Diagnosis of Parkinson's disease, as defined in the UK Brain Bank criteria 2. Hoehn and Yahr stage I-III 3. Participants who are at stable medication regimen 4. Able to walk independently for at least 5 minutes with or without support of accessory device.

Exclusion criteria

1\. Mini Mental State Exam (MMSE) score\< 24

Design outcomes

Primary

MeasureTime frameDescription
Average trunk angle in the sagittal plane using a Postural Analysis Chart8 weeksPostural Analysis

Secondary

MeasureTime frameDescription
Patient satisfaction by VAS scores8 weeksResults for the VAS scores with possible range 0 (worst) to 10 (best)

Countries

Israel

Contacts

Primary ContactMarina Brozgol
marina.brozgol@gmail.com+97236947513
Backup ContactNir Giladi, MD
nirg@tlvmc.gov.il+97236947513

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026