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Recruiting NCT07576114

Comparison of Gluteal Muscle Activation and Core Strengthening in Dead Butt Syndrome Syndrome

No phase Interventional Syndrome

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Group A: Gluteal Muscle Activation, Group B: Gluteal Muscle Activation and Core stregthening exercises.
Who it may be relevant to
Registry conditions: Syndrome. Basic parameters: 18 years — 55 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Pakistan
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Comparison of Gluteal Muscle Activation and Core Strengthening in Dead Butt Syndrome

Overview

The study design would be a Randomized Controlled Trial.This study would include a total 40 participants. 20 participants in each group. Sample size is obtained through G-power. The study duration will be 12 months after the approval from the research board. Non-probability convenience sampling will be used. Randomization will be done through sealed envelope method. The study will be conducted from Quaid-e-Azam Hospital Rawalpindi and Margalla Rehabilitation Centre.

Interventions

  • Other Group A: Gluteal Muscle Activation
    Gluteal Activation focuses on "waking up" and isolating the gluteus maximus, medius, and minimus to ensure they fire properly, often using low-load, high-control movements.
  • Other Group B: Gluteal Muscle Activation and Core stregthening exercises
    Gluteal Activation focuses on "waking up" and isolating the gluteus maximus, medius, and minimus to ensure they fire properly, often using low-load, high-control movements.Core Strengthening focuses on stabilizing the spine and pelvis by targeting the abdominals, back, and deep pelvic muscles.

Primary outcome measures

  • Tampa Scale of Kinesiophobia (TSK-11) [Time frame: 4 weeks]
  • Lower Extremity Functional Scale (LEFS) [Time frame: 4 weeks]
  • Numeric Pain Rating Scale [Time frame: 4 Weeks]
  • The Trendelenburg test [Time frame: 4 Weeks]

Eligibility criteria

Inclusion criteria

  • Symptoms persisting for more than 6 weeks (subacute or chronic cases).
  • Sedentary to moderately active individuals (i.e., not involved in heavy gluteal-strengthening or core training for at least 3 months prior to the study). vParticipants will be diagnosed with Dead Butt Syndrome based on the presence of at least two out of three of the following criteria:
  • Self-reported dull ache, discomfort, or tightness in the gluteal region worsened with prolonged sitting or walking.
  • Positive Trendelenburg Test
  • ≤ 4/5 on the standard MRC grading scale

Exclusion criteria

  • Pregnancy or plans to become pregnant during the study period.
  • Diagnosed hip labral tears, piriformis syndrome, or sciatica unrelated to gluteal amnesia.
  • Degenerative or neurological conditions such as osteoarthritis, multiple sclerosis, stroke, or spinal cord injury.
  • History of significant spinal trauma or surgery in the past 12 months.
  • Engagement in regular physical exercise or participation in rehabilitation programs within the last 6 months.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
Randomized
Model
Parallel assignment
Masking
Open label
Primary purpose
Treatment

Study locations

Pakistan · 1 center
  • Riphah University Islamabad — Islamabad

Identifiers

NCT: NCT07576114 · REC/02289 Rehmat

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗