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Behavioural Intervention
Intervention group for Diabetes
N/A
Recruiting
Research Sponsored by Hamad Medical Corporation
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline and12 weeks
Summary
This trial is proposing the use of plantar electrical stimulation to help improve balance and quality of life in patients with diabetes who are undergoing hemodialysis treatment.
Eligible Conditions
- Cardiovascular Complications
- Diabetes
- Hemodialysis Complication
- Quality of Life
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ baseline and12 weeks
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline and12 weeks
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Change in balance from baseline to 12 weeks
Accidental Falls
Change in gait parameters from baseline to 12 weeks.
+2 moreSecondary study objectives
Change in cognitive function
Change in depression
Change in pain
+1 moreTrial Design
2Treatment groups
Active Control
Placebo Group
Group I: Intervention groupActive Control1 Intervention
The intervention group will take part in a 12-week plantar electrical stimulation intervention using the proposed technology 3 times per week during HD either in a sitting or supine position under the supervision of a research staff member. The duration of each treatment session will be one hour. Patients who receive an activated electrical stimulation unit will receive a standard dose of 30 milliamps as described in the following during each HD session (3 times per week for 12 weeks).
Group II: Control groupPlacebo Group1 Intervention
Placebo controls will have an electrical stimulation unit programmed not to provide any electrical current, while all other lights and programming indicators will be functional. Both active and inactive electrical stimulation units will be programmed to download the period that they are used on a weekly basis in order to verify that the units are used for the prescribed time period.
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Who is running the clinical trial?
Qatar National Research FundUNKNOWN
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221 Total Patients Enrolled
Hamad Medical CorporationLead Sponsor
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