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Superior Cluneal Nerve Entrapment Syndrome, Kinesiotaping and Myofascial Release Techniques

Comparison of the Efficacy of Kinesiotaping and Myofascial Release Techniques in the Treatment of Superior Cluneal Nerve Entrapment Syndrome: A Randomised Single Blind Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06672744
Enrollment
75
Registered
2024-11-04
Start date
2022-08-15
Completion date
2024-08-16
Last updated
2024-11-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Superior Cluneal Nerve Entrapment

Brief summary

Myofascial release techniques and/or kinesiotaping may be effective in the treatment of superior cluneal nerve impingement syndrome ?

Interventions

OTHERExercise

Lumbar muscles (especially quadratus lumborum) and thoracolumbar fascia stretching exercises and strengthening exercises for the lumbar and abdominal muscles were described by the physiotherapist. Participants were asked to perform the exercises three times a day, five days a week

OTHERMyofascial release technique

Myofascial release technique was applied by the same researcher (YY) twice a week for four weeks.

OTHERKinesiotaping

Kinesiotaping was performed by the same researcher (XX) for two sessions per week for four weeks with fascia correction technique

Sponsors

Savaş Karpuz
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* patients diagnosed with superior cluneal nerve entrapment syndrome

Exclusion criteria

* those with communication problems * those who also described pain in the mid-lumbar region

Design outcomes

Primary

MeasureTime frameDescription
Visual Analoque ScaleBefore treatment, immediately after treatment, 1 month after the end of treatmentVisual Analoque Scale is a scale consisting of a single 10 cm line and assesses the intensity of pain. Patients were asked to rate the level of pain after being informed that the beginning point on the scale represented no pain and the end point represented the most excruciating pain they had ever experienced
The Roland-Morris Disability QuestionnaireBefore treatment, immediately after treatment, 1 month after the end of treatmentThe Roland-Morris Disability Questionnaire is a questionnaire developed to assess functional disabilities in patients with low back pain \[15\]. In the questionnaire consisting of 24 sentences about functional disabilities, patients are asked to answer each sentence as yes if it fits their situation and no if it does not. Yes answers are calculated as '1' and no answers as '0' points, resulting in a total score between 0-24, with a higher score indicating more disability.

Secondary

MeasureTime frameDescription
SF-36 Quality of Life ScaleBefore treatment, immediately after treatment, 1 month after the end of treatmentSF-36 Quality of Life Scale is a general quality of life scale frequently used in clinical research. The scale consists of 36 items, which measure 8 different dimensions: physical functions, social functions, role inhibition due to physical problems, physical pain, mental health, role inhibition due to emotional problems, life energy, general health perception. The subscales assess health on a scale of 0 to 100, with higher scores indicating good health quality.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026