Effects of Scapular Exercise on Patients With Scapulocost... | NCT02067598

Studies
Effects of Scapular Exercise on Patients With Scapulocostal Syndrome

NCT02067598

Sponsor

Mae Fah Luang University Hospital

Status

Completed

Last Update Posted

May 6, 2015Estimated

Enrollment

36Actual

Phase

Not Applicable

Conditions

Scapular Pain

Interventions

scapular exercise

Countries

Thailand

Protocol Section

Identification Module Status Module Sponsor/Collaborators Module Oversight Module Description Module Conditions Module Design Module Arms/Interventions Module Outcomes Module Eligibility Module Contacts/Locations Module References Module IPD Sharing Statement Module

Results Section

Participant Flow Module Baseline Characteristics Module Outcome Measures Module Adverse Events Module More Info Module

Annotation Section

Annotation Module

Document Section

Large Document Module

Derived Section

Miscellaneous Info Module Condition Browse Module Intervention Browse Module

Protocol Section

Identification Module

NCT ID

Results Section

No data available

No data is available for this block.

Annotation Section

No data available

No data is available for this block.

Document Section

No data available

No data is available for this block.

Derived Section

Miscellaneous Info Module

Version Holder

Status Module

Record Verification Date

May 2015

Overall Recruitment Status or Expanded Access Status

Completed

Last Known Status

Not provided

Delayed Posting

Not provided

Why Stopped

Not provided

Expanded Access Info

Start Date

Jan 2014

Primary Completion Date

May 2014Actual

Completion Date

May 2014Actual

First Submitted Date

Feb 18, 2014

First Submission Date that Met QC Criteria

Feb 19, 2014

First Posted Date

Feb 20, 2014Estimated

Results Waived

Not provided

Results First Submitted Date

Not provided

Results First Submitted that Met QC Criteria

Not provided

Results First Posted Date

Not provided

Certification/Extension (aka Delayed Results) First Submitted Date

Not provided

Certification/Extension First Submitted that Passed QC Review

Not provided

Certification/Extension First Posted Date

Not provided

Last Update Submitted Date

May 5, 2015

Last Update Posted Date

May 6, 2015Estimated

Sponsor/Collaborators Module

Responsible Party, by Official Title

Dr. Vitsarut Buttagat, Mae Fah Luang University, Mae Fah Luang University HospitalPrincipal Investigator

Lead Sponsor

Mae Fah Luang University HospitalOTHER

Collaborators

Not provided

Oversight Module

Has Data Monitoring Committee (DMC)

Yes

Is FDA Regulated Drug

Not provided

Is FDA Regulated Device

Not provided

Is Unapproved Device

Not provided

Pediatric Postmarket Surveillance of a Device Product

Not provided

Product Exported from US

Not provided

FDAAA801 Violation

Not provided

Description Module

Brief Summary

The purpose of this study is to determine the effect of scapular exercise on pain related parameters including pain intensity, 24 hours pain intensity, pressure pain threshold, anxiety and muscle tension in patients with scapulocostal syndrome.

Detailed Description

Not provided

Design Module

Study Type

Interventional

Number of References to an Expanded Access Study

Not provided

Expanded Access Types

Not provided

Patient Registry

Not provided

Target Follow-Up Duration

Not provided

Phases

Not Applicable

Interventional Study Design

Allocation

Biospecimen

No data available

No data is available for this block.

Enrollment

36Actual

Arms/Interventions Module

Arm Groups

Label	Type	Description	Intervention Names
Scapular exercise	Experimental	The participants will receive thirty minutes session of scapular exercise for 12 sessions	Other: scapular exercise
Control	No Intervention

Interventions

Name	Type	Description	Arm Group Labels	Other Names
scapular exercise	Other		Scapular exercise	The participants will receive thirty minutes session of scapular exercise for 12 sessions

Outcomes Module

Primary Outcomes

Measure	Description	Time Frame
Pressure Pain Threshold as a measure by algometry		6 Weeks

Secondary Outcomes

Measure	Description	Time Frame
Pain scores on visual analog scale		6 weeks
Muscle tension on visual analog scale		6 weeks
Anxiety on State Anxiety Inventory

Other Outcomes

Not provided

Eligibility Module

Eligibility Criteria

Inclusion Criteria:

Male or female
Age between 18 - 50 years old
The participants have experienced spontaneous scapular pain for longer than 12 weeks (chronic) and that at least one trigger point will be present in the scapular region (serratus posterior superior, rhomboid groups, levator scapulae and trapezius muscles). Trigger points will be diagnosed as the presence of focal tenderness in a taut band and with pain recognition (Chatchawan et al., 2005; Tough et al., 2007).
The participants will be able to follow instructions.
Good communication and cooperation.

Exclusion Criteria:

1. A history of the following diseases or disorders:

Rotator cuff disease
Cervical radiculopathy
Degenerative shoulder joint disease
Adhesive capsulitis of shoulder

Accepts Healthy Volunteers

Sex

All

Sex/Gender Based

Not provided

Sex/Gender Description

Not provided

Minimum Age

18 Years

Maximum Age

50 Years

Standard Ages

Adult

Study Population

Not provided

Sampling Method

Not provided

Contacts/Locations Module

Central Contacts

Not provided

Overall Officials

Not provided

Locations

Facility	Status	City	State	ZIP	Country	Contacts
School of Health Science, Mae Fah Luang University		Mueang	Changwat Chiang Rai	57100	Thailand