Effectiveness Taif University P. O. Box 11099 Taif 21944... | NCT05614830

Studies
Effectiveness Taif University P. O. Box 11099 Taif 21944 Effectiveness of Dry Needling in Management of Myofacial Trigger Point

NCT05614830

Sponsor

Taif University

Status

Unknown status

Last Update Posted

Nov 14, 2022Actual

Enrollment

40Estimated

Phase

Not Applicable

Conditions

Myofacial Trigger Points

Interventions

Dry needling ,
usual physical therapy program

Countries

Not provided

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

Nov 2022

Overall Recruitment Status or Expanded Access Status

Unknown status

Last Known Status

Not yet recruiting

Delayed Posting

Not provided

Why Stopped

Not provided

Expanded Access Info

Start Date

Jan 2023Estimated

Primary Completion Date

Jun 2023Estimated

Completion Date

Jun 2023Estimated

First Submitted Date

Nov 6, 2022

First Submission Date that Met QC Criteria

Nov 6, 2022

First Posted Date

Nov 14, 2022Actual

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

Nov 6, 2022

Last Update Posted Date

Nov 14, 2022Actual

Oversight Module

Has Data Monitoring Committee (DMC)

Not provided

Is FDA Regulated Drug

Is FDA Regulated Device

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

myofascial pain syndrome is considered to be a chronic condition due to sensitive pressure points within the muscle recognized as trigger points

Generally the aim of this study will be :

To investigate the effectiveness of dry needling on trigger point in trapezius muscle
Evaluate the pain level before and after the applications of dry needling on trigger points
compare between the effects of dry needling and physical therapy exercise program

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

40Estimated

Arms/Interventions Module

Arm Groups

Label	Type	Description	Intervention Names
Intervention group	Experimental		Other: Dry needling ,
Control group	Active Comparator	Usual physical therapy protocol 4 sessions, two sessions per week each session will include a group of therapeutic exercises	Other: usual physical therapy program

Interventions

Name	Type	Description	Arm Group Labels	Other Names
Dry needling ,	Other	The intervention group will receive sessions of dry needling to relief myofacial pain on trapezius	Intervention group

Outcomes Module

Primary Outcomes

Measure	Description	Time Frame
Pain level	Will be determined using the visuals analogue scale (VAS)	6 weeks
Neck disability index	questionnaire contains 10 items aiming to evaluate the limitation because of neck pain	6 weeks

Secondary Outcomes

Measure	Description	Time Frame
Depression	Will be determined using the Beck's Depression Inventory ( BDI)	6 weeks
Neck Range of motion	Will be measured using CROM

Other Outcomes

Not provided

Eligibility Module

Eligibility Criteria

Inclusion Criteria:

Clinically active trigger point and expression of symptoms of neck pain in trapezius which had lasted for at least 3 months.
Having a pain level higher than 4 and lower than 8 on Visual Analogue Scale ( VAS )
Did not receive any other form of neck treatment during the previous month.

Exclusion Criteria:

Presence of cardiopulmonary disease , the application process requires the subject to be in prone position to expose the area of treatment, this position is un-preferable for cardiopulmonary patients
History of neck surgery
Trigger point treatment in the last 30 days
Any contraindications for dry needling such as local infection, skin disease ,severe postural disorder , tumor , rheumatoid arthritis, cervical spine stenosis and bilateral upper extremity symptoms
pregnancy

Accepts Healthy Volunteers

Sex

All

Sex/Gender Based

Not provided

Sex/Gender Description

Not provided

Minimum Age

18 Years

Maximum Age

Not provided

Standard Ages

AdultOlder Adult

Study Population

Not provided

Sampling Method

Not provided

Intervention Browse Module

MeSH Terms

ID	Term
D000079245	Dry Needling

Ancestor Terms

ID	Term
D000529	Complementary Therapies
D013812	Therapeutics
D026741	Physical Therapy Modalities

Browse Leaves

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Browse Branches

Not provided