Sensorimotor Training for Adults With Diabetic Peripheral Neuropathy
Primary Purpose
Peripheral Neuropathy, Somatosensory Disorders, Sensorimotor Gait Disorder
Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
sensorimotor training based on Feldenkrais method
foot care education
usual care
Sponsored by
About this trial
This is an interventional treatment trial for Peripheral Neuropathy focused on measuring gait, diabetes, sensorimotor training, peripheral neuropathy, somatosensory system, postural control, quality of life, fear of falling, Feldenkrais method
Eligibility Criteria
Inclusion Criteria: having peripheral neuropathy and history of falls or risk factors for it. Current ulcer -
Exclusion Criteria: amputation and cognitive or mental issues
-
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
control
experimental
Arm Description
control arm: usual care and foot care education.
experimental arm: sensorimotor training, foot care education and usual care
Outcomes
Primary Outcome Measures
Cumulative Somatosensory Impairment Index
It measures proprioception, pressure and vibration sensitivity and graphesthesia to sum up somatosensory function in lower legs. Iti is ranging from 0 to 8 being 8 the worst result
Secondary Outcome Measures
Up and Go test
postural control test
Four Square Step test
ability walking in different directions
Tinetti- Performance-Oriented Mobility Assessment (POMA-T)
static and dynamic postural control
Falls Efficacy Scale
It measures the fear of falling, ranging from 0 to 64, being higher scores worst outcome results
SF-36 Health Survey questionnaire , 1.4 version.
Quality of life health-related questionnaire
Validated Spanish version of Short-Form Late-Life Function and Disability Instrument
It measures functional disabilities and frequency of daily life activities, ranging from 31 to 155 and being higher scores better outcome results.
Full Information
NCT ID
NCT05262946
First Posted
January 31, 2022
Last Updated
November 3, 2022
Sponsor
Universidad Complutense de Madrid
1. Study Identification
Unique Protocol Identification Number
NCT05262946
Brief Title
Sensorimotor Training for Adults With Diabetic Peripheral Neuropathy
Official Title
Somatosensory Restoration and Postural Control Improvement in People With Diabetic Peripheral Neuropathy Applying Sensorimotor Training: a Multicentric Randomized Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
March 2021
Overall Recruitment Status
Completed
Study Start Date
January 1, 2016 (Actual)
Primary Completion Date
December 22, 2019 (Actual)
Study Completion Date
January 30, 2022 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Universidad Complutense de Madrid
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
Adults with diabetic peripheral neuropathy tend to fall more frequently than healthy population as a consequence of multiple sensorimotor and cognitive damages. In this protocol study, a randomized controlled trial is proposed using a sensorimotor intervention based on Feldenkrais method to improve somatosensory aspects and, therefore, postural control of participants.
Detailed Description
Among all the systems suffering damage due to hyperglucemia toxicity in diabetes, somatosensory system, composed by proprioception and skin sensory receptors has a key role since it is in charge of the faster body reaction when a postural control response is needed. Despite of it, few studies have focused on this issue. This randomized controlled trial proposed a safe and easy training adapted to adults and old people with diabetic peripheral neuropathy. Pressure, touch, proprioception and graphesthesia sensibility were measured, as well as functionality in daily basis, quality of life and fear of falling.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Peripheral Neuropathy, Somatosensory Disorders, Sensorimotor Gait Disorder
Keywords
gait, diabetes, sensorimotor training, peripheral neuropathy, somatosensory system, postural control, quality of life, fear of falling, Feldenkrais method
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
2 arms and single blinded randomized controlled trial
Masking
InvestigatorOutcomes Assessor
Masking Description
measurements and statistical analysis were made without knowing who participated in control or experimental group
Allocation
Randomized
Enrollment
44 (Actual)
8. Arms, Groups, and Interventions
Arm Title
control
Arm Type
Active Comparator
Arm Description
control arm: usual care and foot care education.
Arm Title
experimental
Arm Type
Experimental
Arm Description
experimental arm: sensorimotor training, foot care education and usual care
Intervention Type
Behavioral
Intervention Name(s)
sensorimotor training based on Feldenkrais method
Intervention Description
8 weeks of balance and sensorimotor training twice a week
Intervention Type
Behavioral
Intervention Name(s)
foot care education
Intervention Description
Recommendations for preventing foot ulcers
Intervention Type
Combination Product
Intervention Name(s)
usual care
Intervention Description
drugs and diet usual care
Primary Outcome Measure Information:
Title
Cumulative Somatosensory Impairment Index
Description
It measures proprioception, pressure and vibration sensitivity and graphesthesia to sum up somatosensory function in lower legs. Iti is ranging from 0 to 8 being 8 the worst result
Time Frame
2 years
Secondary Outcome Measure Information:
Title
Up and Go test
Description
postural control test
Time Frame
2 years
Title
Four Square Step test
Description
ability walking in different directions
Time Frame
2 years
Title
Tinetti- Performance-Oriented Mobility Assessment (POMA-T)
Description
static and dynamic postural control
Time Frame
2 years
Title
Falls Efficacy Scale
Description
It measures the fear of falling, ranging from 0 to 64, being higher scores worst outcome results
Time Frame
2 years
Title
SF-36 Health Survey questionnaire , 1.4 version.
Description
Quality of life health-related questionnaire
Time Frame
2 years
Title
Validated Spanish version of Short-Form Late-Life Function and Disability Instrument
Description
It measures functional disabilities and frequency of daily life activities, ranging from 31 to 155 and being higher scores better outcome results.
Time Frame
2 years
10. Eligibility
Sex
All
Minimum Age & Unit of Time
55 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: having peripheral neuropathy and history of falls or risk factors for it. Current ulcer -
Exclusion Criteria: amputation and cognitive or mental issues
-
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
MARIA TERESA ANGULO CARRERA, DR
Organizational Affiliation
UNIVERSIDAD COMPLUTENSE MADRID
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
NOEMI GONZALEZ PEREZ DE VILLAR, DR
Organizational Affiliation
HOSPITAL UNIVERSITARIO DE LA PAZ
Official's Role
Study Director
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Sensorimotor Training for Adults With Diabetic Peripheral Neuropathy
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