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TENS for Chronic Pain
N/A
Recruiting
Led By Guillaume Léonard, PhD
Research Sponsored by Université de Sherbrooke
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Being off work completely due to a musculoskeletal injury
Being 55 years of age or older
Must not have
Having already experimented with TENS
Being diagnosed with cancer
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 4 months
Summary
This trial is testing whether a remote rehabilitation intervention combining therapeutic exercises and electrical nerve stimulation (TENS) can help people aged 55 and over who have stopped working due to pain. Different feasibility indicators and clinical measures will be used to evaluate the effect of the intervention.
Who is the study for?
This trial is for individuals aged 55 or older who are off work due to musculoskeletal injuries, starting physical rehab, and can handle basic tech like video calls and texts. They should speak French, have stable medication routines, mild to moderate pain during movement, and not have used TENS before.
What is being tested?
The study tests if combining therapeutic exercises with real or placebo TENS via telerehabilitation helps in work rehabilitation for older adults. It's a triple-blind study where neither participants nor researchers know who gets the real treatment until after the results.
What are the potential side effects?
TENS is generally safe but may cause skin irritation at the electrode sites or muscle twitching. Some people might feel uncomfortable sensations from the electrical current.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
I am currently not working due to a musculoskeletal injury.
Select...
I am 55 years old or older.
Exclusion Criteria
You may be eligible for the trial if you check “No” for criteria below:Select...
I have tried using a TENS unit for pain relief.
Select...
I have been diagnosed with cancer.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 4 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~4 months
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
Adherence rate
Attrition rate
Exclusion rate
+3 moreSecondary study objectives
Disability in work Rehabilitation
Overall treatment satisfaction
Pain catastrophizing
+5 moreTrial Design
2Treatment groups
Experimental Treatment
Placebo Group
Group I: Intervention groupExperimental Treatment1 Intervention
Real TENS and personalized exercise program in telerehabilitation (3 sessions/week over 3 weeks) n = 12
Group II: Control groupPlacebo Group1 Intervention
Simulated TENS and personalized exercise program in telerehabilitation (3 sessions/week over 3 weeks) n = 12
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
TENS
2011
Completed Phase 2
~2040
Find a Location
Who is running the clinical trial?
Réseau québécois de recherche sur le vieillissement (RQRV)UNKNOWN
1 Previous Clinical Trials
32 Total Patients Enrolled
Université de SherbrookeLead Sponsor
304 Previous Clinical Trials
76,705 Total Patients Enrolled
11 Trials studying Chronic Pain
1,124 Patients Enrolled for Chronic Pain
Réseau Provincial De Recherche En Adaptation-Réadaptation (REPAR)UNKNOWN
1 Previous Clinical Trials
37 Total Patients Enrolled
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I can speak French.I am currently not working due to a musculoskeletal injury.I have tried using a TENS unit for pain relief.My pain level is between 1 and 6 when moving.I am 55 years old or older.I have been diagnosed with cancer.
Research Study Groups:
This trial has the following groups:- Group 1: Control group
- Group 2: Intervention group
Awards:
This trial has 0 awards, including:Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
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