Gluteus Medius Latent Trigger Point and Muscle Strength in Healthy Subjects
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| ClinicalTrials.gov Identifier: NCT04640558 |
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Recruitment Status :
Completed
First Posted : November 23, 2020
Last Update Posted : January 29, 2021
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| Condition or disease | Intervention/treatment |
|---|---|
| Myofascial Pain Syndrome Muscle Weakness | Device: Muscle strength measurement |
| Study Type : | Observational [Patient Registry] |
| Actual Enrollment : | 48 participants |
| Observational Model: | Other |
| Time Perspective: | Prospective |
| Target Follow-Up Duration: | 4 Weeks |
| Official Title: | The Relationship Between Gluteus Medius Latent Trigger Point and Muscle Strength in Healthy Subjects |
| Actual Study Start Date : | November 17, 2020 |
| Actual Primary Completion Date : | January 17, 2021 |
| Actual Study Completion Date : | January 17, 2021 |
| Group/Cohort | Intervention/treatment |
|---|---|
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Group 1. Latent Myofascial Trigger Point Group
24 participants who will be clinically diagnosed with unilateral latent myofascial trigger point in the dominant side gluteus medius muscle.
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Device: Muscle strength measurement
The bilateral gluteus medius muscle strength of each participant will be measured by the assessor (MB) blinded to the participants using the Lafayette manual muscle tester. (Lafayette Instrument Company, Lafayette IN, USA). In the participant's side-lying position, the practitioner applied resistance from the upper ankle to the abduction movement with slight flexion of the upper hip. During the measurements, the participants were asked to perform the maximum isometric contraction for 3 seconds. Gluteus medius muscle strength measurements were repeated three times, one minute apart, on the right and left sides. The mean of the measurements was calculated and recorded |
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Group 2. Non-Latent Myofascial Trigger Point Group
24 participants who don't have latent myofascial trigger point.
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Device: Muscle strength measurement
The bilateral gluteus medius muscle strength of each participant will be measured by the assessor (MB) blinded to the participants using the Lafayette manual muscle tester. (Lafayette Instrument Company, Lafayette IN, USA). In the participant's side-lying position, the practitioner applied resistance from the upper ankle to the abduction movement with slight flexion of the upper hip. During the measurements, the participants were asked to perform the maximum isometric contraction for 3 seconds. Gluteus medius muscle strength measurements were repeated three times, one minute apart, on the right and left sides. The mean of the measurements was calculated and recorded |
- Gluteus medius muscle strength [ Time Frame: One month ]In the participant's side-lying position, the practitioner will be applied resistance from the upper ankle to the abduction movement with slight flexion of the upper hip. During the measurements, the participants will be asked to perform the maximum isometric contraction for 3 seconds. Gluteus medius muscle strength measurements will be repeated three times, one minute apart, on the right and left sides. The mean of the measurements will be calculated and recorded
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| Ages Eligible for Study: | 18 Years to 40 Years (Adult) |
| Sexes Eligible for Study: | Male |
| Sampling Method: | Probability Sample |
Inclusion Criteria:
- Patient age: 18-40 years.
- Absence of musculoskeletal complaints related to the lumbar, sacroiliac, and hip area.
- Absence of bilateral latent MTrP in the gluteus medius muscle.
- Latent trigger point in the gluteus medius muscle on the dominant side with palpation.
Exclusion Criteria:
- A history of medical treatment, physical therapy, injection therapy, or surgical treatment related to the lumbar, sacroiliac, and hip area.
- History of trauma, or malignancy or being pregnant, or if the patient is in the lactation period.
- Bilateral latent MTrP in the gluteus medius muscle.
- Presence of latent MTrP on the non-dominant side.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT04640558
| Turkey | |
| Biruni University Faculty of Medicine | |
| İstanbul, Turkey, 34100 | |
| Responsible Party: | Fatih Bagcier, Medical Doctor, Kars State Hospital |
| ClinicalTrials.gov Identifier: | NCT04640558 |
| Other Study ID Numbers: |
KarsSH |
| First Posted: | November 23, 2020 Key Record Dates |
| Last Update Posted: | January 29, 2021 |
| Last Verified: | January 2021 |
| Individual Participant Data (IPD) Sharing Statement: | |
| Plan to Share IPD: | No |
| Studies a U.S. FDA-regulated Drug Product: | No |
| Studies a U.S. FDA-regulated Device Product: | No |
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Trigger point Gluteus medius muscle |
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Muscle Weakness Myofascial Pain Syndromes Fibromyalgia Muscular Diseases Musculoskeletal Diseases Neuromuscular Manifestations |
Neurologic Manifestations Nervous System Diseases Pathologic Processes Rheumatic Diseases Neuromuscular Diseases |

