Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05085236
Other study ID # CMUH110-REC2-124
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date November 26, 2021
Est. completion date August 26, 2023

Study information

Verified date December 2022
Source China Medical University Hospital
Contact Li-Wei Chou, PhD
Phone +886-4-22052121
Email chouliwe@mail.cmuh.org.tw
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The post-stroke survivors suffered from shoulder pain are very common. The investigators performed Fu's subcutaneous needling (FSN). This experiment used a randomized controlled trial to assess the immediate, short-term and long-term effects of Fu's subcutaneous needling therapy on hemiplegic shoulder pain in patient with stroke.


Description:

The prevalence of complication in post-stroke survivors is 30-96%. Post-stroke pain is the most common complication. According to previous researches there are sixty percent post-stroke survivors who suffered from upper limb pain. The mechanism causes post-stroke shoulder pain is imbalance of shoulder muscles and in-coordination of shoulder motor control due to cerebral vascular disease. Post-stroke shoulder pain often causes the limitation of shoulder range of motion, and the pain always affected quality of life and daily activities. Because of shoulder pain, those post-stroke survivors postponed the program of rehabilitation. The treatments of post-stroke shoulder pain are transcutaneous electrical nerve stimulation, drug, intra-articular injection and nerve block. Acupuncture with combination of rehabilitation has been proved by many researches in alleviating pain and increasing quality of life in treating post-stroke shoulder pain. Fu's subcutaneous needling is a newly technique based on meridian theory and the technique is used to treat cervical, lumbar and four limb's pain proved by many researches. Fu's subcutaneous needling in managing post-stroke pain has less reported, so investigator set up a proposal to see if the Fu's subcutaneous needling could elevate more therapeutic effect compared to usual care or not. The investigators will enroll patients into two groups, experimental and control groups. The interventions in experimental group are Fu's subcutaneous needling in combination with rehabilitation, and in control group is rehabilitation. The trial will extend two weeks, and investigator will treat with Fu's subcutaneous needling three times in the first, second and fourth day when the patients include to our trial. The outcome measurements are visual analog scale, range of motion of shoulder, pressure pain threshold of myofascial trigger point, acromion-greater tuberosity distance, Fugl-Meyer assessment in upper extremity and functional independence measure.


Recruitment information / eligibility

Status Recruiting
Enrollment 60
Est. completion date August 26, 2023
Est. primary completion date August 26, 2023
Accepts healthy volunteers No
Gender All
Age group 40 Years and older
Eligibility Inclusion Criteria: - 1. Volunteers who are older than 40 years old suffered from first stroke attack including infarction and hemorrhage with image proved and can cooperate with the experiment. - 2. Stroke patient suffered from shoulder pain. - 3. Patient can follow the directions of Fu's subcutaneous needling and regular rehabilitation program. Exclusion Criteria: - 1. There are contraindications to general treatment, such as serious medical problems, recent serious trauma, or pregnant and lactated women. - 2. There has been a history of drug abuse (including excess alcohol) that affects pain assessment. - 3. Cognitive impairment, unable to cooperate with the experiment. - 4. Aphasia - 5. Have received shoulder joint injection in recent 6 months. - 6. Have serious skin infection, laceration, wound and trauma.

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Fu's subcutaneous needling (FSN)
physician will use a disposable Fu's subcutaneous needling (FSN) to penetrate the subject's skin in the middle from elbow lateral epicondyle to radial styloid process. Then physician will push forward the needle parallel to the skin surface. the physician will sway the needle 100 times in a minute. After procedure of swaying needle, the physician will instruct subject to do several movements, and each movement will perform 10 seconds and rest 10 seconds for 3 repetitions. The movements are active isometric elbow flexion, active isometric shoulder internal rotation, passive shoulder external and internal rotation. After above re-perfusion approach of muscles, the physician will take out the needle to finish the treatment.
Rehabilitation
Rehabilitation mentioned here is the regular rehabilitation programs for treating post-stroke hemiplegic shoulder pain prescribed by the rehabilitation physician.

Locations

Country Name City State
Taiwan China Medical University Hospital Taichung

Sponsors (1)

Lead Sponsor Collaborator
China Medical University Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Visual Analog Scale A Visual Analog Scale consists of a line, often 10 cm long, with verbal anchors at either end, on left of line, zero, meant no pain otherwise on right, 10, meant strong pain. The patient places a mark at a point on the line corresponding to the patient's rating of pain intensity. 1 day
Primary Pressure Pain Threshold Pressure pain threshold (PPT) is defined as the minimum force applied which induces pain. This measure has proven to be commonly useful in evaluating tenderness symptom 1 day
Primary Range of Motion of Shoulder Range of Motion is the measurement of movement around a specific joint, measured in degrees of a circle. In this study we measure shoulder joint, glenohumeral joint, in flexion, extension, external and internal rotation. 1 day
Primary Acromion-GreaterTuberosity Distance In this study we assess of shoulder joint subluxation by means of ultrasound measurement of Acromion-greater tuberosity distance. 1 day
Primary Fugl-Meyer assessment in upper extremity The Fugl-Meyer Assessment (FMA) is a stroke-specific, performance-based impairment index. In upper extremity, we measure motor function included shoulder, elbow, wrist and hand, and assess coordination using finger to nose. 1 day
Primary Functional Independence Measure The Functional Independence Measure (FIM) is an instrument that was developed as a measure of disability. Includes measures of independence for self-care, including sphincter control, transfers, locomotion, communication, and social cognition. 1 day
See also
  Status Clinical Trial Phase
Recruiting NCT01572285 - Transforaminal Epidural Steroid Injection to Treat Hemiplegic Shoulder Pain N/A
Recruiting NCT05395325 - Clinical Effects of Combined Kinesiotaping and Steroid Injection in Stroke Patients With Hemiplegic Shoulder Pain N/A
Recruiting NCT06098508 - Osteopathic Manual Treatment for Hemiplegic Shoulder Pain and Upper Extremity Function in Stroke Patients N/A
Completed NCT04292613 - "The Effect of Hemiplegic Shoulder Pain on Balance, Upper Extremity Function and Quality of Life"
Completed NCT04933318 - Effects of TENS and Interference on Pain, Functional Status and Range of Motion in Shoulder Pain in Stroke Patients N/A
Completed NCT06407596 - HILT or Conventional Combined Physical Therapy, in the Management of Hemiplegic Shoulder Pain N/A
Recruiting NCT04128605 - Suprascapular Nerve Block Versus Intraarticular Steroid Injection in Hemiplegic Shoulder Pain N/A
Terminated NCT03093935 - StimRouterâ„¢ for Pain Management in Post-stroke Shoulder Pain N/A
Recruiting NCT04758182 - Effects of High Intensity Laser Therapy Compared With Ultrasound Therapy on Hemiplegic Shoulder Pain; Randomized Control Trial N/A
Completed NCT04768140 - Bobath Approach On Hemiplegic Shoulder Pain N/A
Completed NCT01847885 - Electrical Stimulation for the Treatment of Chronic Post-Stroke Shoulder Pain Using the Smartpatch System N/A