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Non-surgical Treatment of Carpal Tunnel Syndrome by Means of Mechanical Traction (MT-CTS)

Primary Purpose

Carpal Tunnel Syndrome

Status
Completed
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
mechanical traction
Care as usual
Sponsored by
Tilburg University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Carpal Tunnel Syndrome focused on measuring carpal tunnel syndrome, traction, mechanical traction, Phystrac

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • diagnosed with CTS using electrodiagnostic testing
  • being physically capable of visiting the outpatient clinic in Venlo twice per week
  • being physically capable of sitting in upright position in a chair for 10-20 minutes, twice per week
  • not intending to move outside the area within 3 months after inclusion

Exclusion Criteria:

  • not understanding Dutch appropriately
  • other known (rare) cause of neuropathy
  • suffering from severe psychiatric disorders, such as personality disorder, schizophrenia or bipolar disorder

Sites / Locations

  • Viecuri Medisch Centrum

Arms of the Study

Arm 1

Arm 2

Arm Type

Other

Experimental

Arm Label

Care as usual

Mechanical traction

Arm Description

The patient will receive the usual care provided by the neurologists at VieCuri Medical Center. This may include an expectant strategy, a wrist splint, corticosteroid injection or carpal tunnel release surgery.

Twelve treatments with mechanical traction using the Phystrac traction apparatus.

Outcomes

Primary Outcome Measures

Change from baseline in symptom severity and functional status on the Boston Carpal Tunnel Questionnaire (BCTQ) at 12 months
Functional status and symptom severity will be measured using a self-reported scale: the BCTQ. The BCTQ is a disease-specific questionnaire and consists of two different scales: the Symptom Severity Scale (SSS) and the Functional Status Scale (FSS). The SSS consists of 11 questions about symptom severity. The FSS consists of 8 daily activities which are rated based on degree of difficulty. The SSS and the FSS are rated on a five-point scale, where a higher score represents a greater impairment.

Secondary Outcome Measures

Change from baseline in quality of life on abbreviated version of the World Health Organisation Quality of Life (WHOQOL-BREF)
Self-reported quality of life will be measured using the WHOQOL-BREF in Dutch. It consists of 26 items which can be scored on a five-point scale. Better quality of life is represented by a higher score.
Change from baseline in absenteeism from work
A non-standardized questionnaire is used to collect the number of days off work of each patient. Patients are also asked if they are currently on sick leave or have been because of their CTS complaints.
Change from baseline in health care related resource utilization
A non-standardized questionnaire is used to assess if patients have visited a professional caregiver (general practitioner, physiotherapist, psychologist, etc.) in the past 12 months, if they spent time in the hospital or use medication.

Full Information

First Posted
September 19, 2013
Last Updated
December 8, 2016
Sponsor
Tilburg University
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1. Study Identification

Unique Protocol Identification Number
NCT01949493
Brief Title
Non-surgical Treatment of Carpal Tunnel Syndrome by Means of Mechanical Traction
Acronym
MT-CTS
Official Title
Study of the Effectiveness of Mechanical Traction as a Non-Surgical Treatment for Carpal Tunnel Syndrome Compared to Care as Usual: a Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
December 2016
Overall Recruitment Status
Completed
Study Start Date
October 2013 (undefined)
Primary Completion Date
June 2016 (Actual)
Study Completion Date
June 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Tilburg University

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The objective of this study is to evaluate the effectiveness of mechanical traction in patients with Carpal Tunnel Syndrome compared to care as usual.
Detailed Description
This randomized controlled trial will examine the effectiveness of mechanical traction compared to care as usual as a non-surgical treatment for Carpal Tunnel Syndrome (CTS). Patients diagnosed with CTS are recruited from the outpatient neurology clinic of VieCuri Medical Center in Venlo, The Netherlands. They will be randomly assigned to the intervention or control group. Patients in the intervention group will receive 12 treatments with mechanical traction during six consecutive weeks. Patients in the control group will receive care as usual, which can include splinting, a corticosteroid injection, carpal tunnel release surgery or an expectant strategy. Outcomes will be assessed at baseline and at 3, 6, and 12 months after inclusion.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Carpal Tunnel Syndrome
Keywords
carpal tunnel syndrome, traction, mechanical traction, Phystrac

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
181 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Care as usual
Arm Type
Other
Arm Description
The patient will receive the usual care provided by the neurologists at VieCuri Medical Center. This may include an expectant strategy, a wrist splint, corticosteroid injection or carpal tunnel release surgery.
Arm Title
Mechanical traction
Arm Type
Experimental
Arm Description
Twelve treatments with mechanical traction using the Phystrac traction apparatus.
Intervention Type
Device
Intervention Name(s)
mechanical traction
Other Intervention Name(s)
Phystrac mechanical traction device (type GR 10)
Intervention Description
Twelve treatments with mechanical traction using the Phystrac traction apparatus. The Phystrac provides traction to the wrist using weights between 1 and 18 kg. The weights provide a pulling force in line with the forearm. After 8 seconds the weight is lifted, and there is a rest period of 4 seconds. This cycle will be repeated 10 times. Another two sets of 10 traction movements will be applied with the wrist positioned in 30 degrees supination and 30 degrees pronation. In total, 30 traction movements will be applied during each treatment.
Intervention Type
Other
Intervention Name(s)
Care as usual
Intervention Description
Usual care provided by the neurologist (e.g. corticosteroid injection, wrist splint, carpal tunnel release surgery).
Primary Outcome Measure Information:
Title
Change from baseline in symptom severity and functional status on the Boston Carpal Tunnel Questionnaire (BCTQ) at 12 months
Description
Functional status and symptom severity will be measured using a self-reported scale: the BCTQ. The BCTQ is a disease-specific questionnaire and consists of two different scales: the Symptom Severity Scale (SSS) and the Functional Status Scale (FSS). The SSS consists of 11 questions about symptom severity. The FSS consists of 8 daily activities which are rated based on degree of difficulty. The SSS and the FSS are rated on a five-point scale, where a higher score represents a greater impairment.
Time Frame
Baseline, 3 and 6 weeks (intervention group) and 3, 6 and 12 months.
Secondary Outcome Measure Information:
Title
Change from baseline in quality of life on abbreviated version of the World Health Organisation Quality of Life (WHOQOL-BREF)
Description
Self-reported quality of life will be measured using the WHOQOL-BREF in Dutch. It consists of 26 items which can be scored on a five-point scale. Better quality of life is represented by a higher score.
Time Frame
Baseline, 6 weeks (intervention group) and 3, 6 and 12 months.
Title
Change from baseline in absenteeism from work
Description
A non-standardized questionnaire is used to collect the number of days off work of each patient. Patients are also asked if they are currently on sick leave or have been because of their CTS complaints.
Time Frame
Baseline, 3 and 6 weeks (intervention group) and 3, 6 and 12 months.
Title
Change from baseline in health care related resource utilization
Description
A non-standardized questionnaire is used to assess if patients have visited a professional caregiver (general practitioner, physiotherapist, psychologist, etc.) in the past 12 months, if they spent time in the hospital or use medication.
Time Frame
Baseline, 3 and 6 weeks (intervention group) and 3, 6 and 12 months.
Other Pre-specified Outcome Measures:
Title
Change from baseline in depression and anxiety on the 4-item Patient Health Questionnaire (PHQ-4)
Description
Self-reported depression and anxiety is measured using the PHQ-4. The questionnaire consists of 2 items on depression and 2 on anxiety answered on a 4-point scale, where a higher score represents a higher level of anxiety and depression.
Time Frame
Baseline, 6 weeks (intervention groups and 3, 6, and 12 months.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: diagnosed with CTS using electrodiagnostic testing being physically capable of visiting the outpatient clinic in Venlo twice per week being physically capable of sitting in upright position in a chair for 10-20 minutes, twice per week not intending to move outside the area within 3 months after inclusion Exclusion Criteria: not understanding Dutch appropriately other known (rare) cause of neuropathy suffering from severe psychiatric disorders, such as personality disorder, schizophrenia or bipolar disorder
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Victor Pop, Prof. Dr.
Organizational Affiliation
Tilburg University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Viecuri Medisch Centrum
City
Venlo
State/Province
Limburg
ZIP/Postal Code
5912 BL
Country
Netherlands

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
34552548
Citation
Meems M, Boekhorst MGBM, Pop VJM. Long-Term Follow-Up Results of Mechanical Wrist Traction as Non-Invasive Treatment for Carpal Tunnel Syndrome. Front Neurol. 2021 Sep 6;12:668549. doi: 10.3389/fneur.2021.668549. eCollection 2021.
Results Reference
derived

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Non-surgical Treatment of Carpal Tunnel Syndrome by Means of Mechanical Traction

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