Clinical Massage Therapy as a Treatment for Carpal Tunnel Syndrome

NCT ID: NCT02706418

Last Updated: 2018-02-28

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

6 participants

Study Classification

INTERVENTIONAL

Study Start Date

2016-12-31

Study Completion Date

2017-08-31

Brief Summary

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Once participants have been recruited, their grip strength shall be tested and they will all complete baseline questionnaires to assess functional status and symptom severity.

Following the recruitment stage, participants will be asked to attend Medway Maritime Hospital once a week for four weeks, to receive the massage protocol. At the first session participants shall be asked to rate their pain (NPRS), before receiving a massage treatment. This will be followed by instructions on how to perform self-massage, which they will be asked to complete daily over the four-week period, and record in a diary. At the remaining three sessions, participants shall just complete the NPRS prior to receiving the massage treatment.

After four weeks the group will be reassessed at the same Orthopaedic Clinic they attended prior to recruitment. They will be asked to complete a final pain score, record any changes in their condition, repeat the initial symptom questionnaire, and finally preform a grip strength test. The duration of four weeks was chosen as this is the time-frame within which the specific massage protocol advises a 'significant symptom improvement' should be seen.

Detailed Description

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Conditions

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Carpal Tunnel Syndrome

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Clinical Massage Therapy

Group Type OTHER

Clinical Massage Therapy

Intervention Type PROCEDURE

Interventions

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Clinical Massage Therapy

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Aged 18 years or above.
* Pain paraesthesia and/or hypoesthesia in the hand, in the area innervated by the median nerve.
* Participants must have a clinical diagnosis of Carpal Tunnel Syndrome (CTS).
* Participant must be able to comply with the study procedures.
* Participant must have attended the Medway Maritime Hospital (Kent), for assessment of the present condition.
* Participant is willing and able to give informed consent for participation in the study.
* Participant must not be contra-indicated for the receipt of massage.
* Participants must be able to speak and read English fluently.

Exclusion Criteria

* Participants who are receiving any additional treatment for their carpal tunnel pain that is not part of standard care (topical pain relief, bracing).
* Participants that have had any surgery on the anatomical sites relevant to the condition and/or treatment (neck, shoulder, arm, wrist, hand).
* Participants that have any suggestion of an additional condition related to carpal tunnel pain (i.e. previous trauma, pregnancy, etc).
* Planning to undertake any activities or lifestyle changes which may affect their levels of carpal tunnel pain (e.g. changing/ceasing occupation, alternative symptom therapy, adopting/ceasing a hobby).
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Medway NHS Foundation Trust

OTHER

Sponsor Role collaborator

Jing Advanced Massage Training

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Medway Maritime Hospital

Gillingham, Kent, United Kingdom

Site Status

Countries

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United Kingdom

Other Identifiers

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CTS-01

Identifier Type: -

Identifier Source: org_study_id

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