Dry Needling Treatment in Hemiplegic Shoulder Pain

NCT ID: NCT04790071

Last Updated: 2023-06-12

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

46 participants

Study Classification

INTERVENTIONAL

Study Start Date

2022-10-01

Study Completion Date

2023-04-09

Brief Summary

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To evaluate the efficacy of dry needling therapy on shoulder pain and upper extremity functions in hemiplegic patients.

Detailed Description

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The myofascial trigger point is an overlooked issue in hemiplegic shoulder pain. Our aim in this study is to evaluate whether dry needling treatment contributes to the conventional treatment approach.

Conditions

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Hemiplegia Shoulder Pain Myofascial Pain

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Prospective randomised controlled
Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Outcome Assessors

Study Groups

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Conventional therapy

It covers the classical physical therapy modalities that patients will take for shoulder pain.

Group Type ACTIVE_COMPARATOR

Conventional physical therapy

Intervention Type OTHER

Conventional physical therapy: The patients received physical therapy to the shoulder, transcutaneous electrical nerve stimulation, and stretching and strengthening exercises (5 days per week for three weeks in a total of 15 sessions).

Conventional therapy plus dry needling

It covers the classical physical therapy modalities that patients will take for shoulder pain. It also refers to the dry needling treatment to be applied.

Group Type ACTIVE_COMPARATOR

Conventional physical therapy plus dry needling

Intervention Type OTHER

Conventional physical therapy plus dry needling: The patients received physical therapy to the shoulder, including transcutaneous electrical nerve stimulation, stretching, and strengthening exercise (5 days per week for three weeks in a total of 15 sessions). And also, a total of 3 dry needling sessions were applied at 7-day intervals.

Interventions

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Conventional physical therapy

Conventional physical therapy: The patients received physical therapy to the shoulder, transcutaneous electrical nerve stimulation, and stretching and strengthening exercises (5 days per week for three weeks in a total of 15 sessions).

Intervention Type OTHER

Conventional physical therapy plus dry needling

Conventional physical therapy plus dry needling: The patients received physical therapy to the shoulder, including transcutaneous electrical nerve stimulation, stretching, and strengthening exercise (5 days per week for three weeks in a total of 15 sessions). And also, a total of 3 dry needling sessions were applied at 7-day intervals.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* The patients included in the study were aged between 30-60 years, with at least a 3-month history of hemorrhagic or ischemic stroke.

Exclusion Criteria

* if they had severe difficulty in communication
* had received a corticosteroid injection within 3 months prior to enrollment
* had bleeding diathesis, a history of shoulder surgery
* a preexisting painful shoulder disorder, or had a cardiac pacemaker.
Minimum Eligible Age

30 Years

Maximum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Kars State Hospital

OTHER

Sponsor Role lead

Responsible Party

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Fatih Bagcier

Study Principal Investigator

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Fatih Bagcier

Role: PRINCIPAL_INVESTIGATOR

Kars State Hospital

Locations

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Kars State Hosital

Kars, , Turkey (Türkiye)

Site Status

Kars State Hospital

Kars, , Turkey (Türkiye)

Site Status

Countries

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Turkey (Türkiye)

References

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Bagcier F, Yurdakul OV, Deniz G, Akbulut A, Celik Y, Temel MH. Is Dry Needling Treatment an Extra Contribution to Conventional Treatment for Hemiplegic Shoulder Pain? A Prospective, Randomized Controlled Study. Med Acupunct. 2023 Oct 1;35(5):236-245. doi: 10.1089/acu.2023.0060. Epub 2023 Oct 17.

Reference Type DERIVED
PMID: 37900876 (View on PubMed)

Other Identifiers

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2015-KAEK-43-20-12

Identifier Type: -

Identifier Source: org_study_id

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