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Clinical Trials/NCT04726423
NCT04726423
Recruiting
Not Applicable

Reduce Chronic Pain With Transcranial Direct Current Stimulation in Clinical Settings

Université de Sherbrooke1 site in 1 country30 target enrollmentJanuary 4, 2021
ConditionsChronic Pain

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Chronic Pain
Sponsor
Université de Sherbrooke
Enrollment
30
Locations
1
Primary Endpoint
Change in Beck Depression Inventory
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

Physical exercises and transcranial direct current stimulation (tDCS) are both known to reduce chronic pain in structured laboratory studies. The aim of this study is to assess the efficacy of this combined treatment in clinical settings.

Detailed Description

Chronic pain patients who are going to the physiotherapy clinic to receive tDCS treatment sessions are evaluated in order to assess the efficacy of tDCS in clinical settings. Physiotherapists prescribe physical exercises adapted to the patients conditions. Patients performed their physical exercises every time they received a tDCS treatment, but were also recommended to continue their physical exercises program at home after completion of physiotherapy visits. Concerning tDCS treatment, patients were encouraged to receive 1 tDCS session per day for 5 consecutive days.

Registry
clinicaltrials.gov
Start Date
January 4, 2021
End Date
December 2023
Last Updated
2 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Guillaume Léonard

Professor

Université de Sherbrooke

Eligibility Criteria

Inclusion Criteria

  • To have chronic pain

Exclusion Criteria

  • Contraindication to tDCS

Outcomes

Primary Outcomes

Change in Beck Depression Inventory

Time Frame: Baseline, 1 week, 1 month

Depression

Change in Patient global impression of change

Time Frame: 1 week, 1 month

Impression of change

Change in Brief Pain Inventory

Time Frame: Baseline, 1 week, 1 month

Physical Function

Change in McGill pain Questionnaire

Time Frame: Baseline, 1 week, 1 month

qualitative and quantitative aspects of pain

Change in Tampa Questionnaire

Time Frame: Baseline, 1 week, 1 month

Kinesiophobia

Secondary Outcomes

  • Side effect(Through study completion, an average of 5 days)
  • Number of sessions received(Through study completion, an average of 5 days)

Study Sites (1)

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