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The purpose of this study is to evaluate the comparative effects of post-isometric relaxation (PIR) and active isolated stretch (AIS) techniques on reducing pain, improving range of motion, and decreasing functional disability in individuals with piriformis syndrome. A total of 40 participants will be recruited, aged 20-55 yrs, with confirmed piriformis syndrome. Participants will be randomized into two equal groups. Group A (post isometric relaxation) and Group B (active isolated stretch). Both groups will receive Conventional Therapy (Thermotherapy, Electrotherapy).
Study variables include:
The intervention will last 2 weeks with 6 sessions (3 sessions per week). Assessments will be conducted at baseline (Week 1, Pre-treatment) and Post every second session. Data will be analyzed to compare immediate and short-term effects of the two interventions.
This study aims to provide evidence for targeted manual therapy approaches in priformis syndrome, potentially guiding clinicians toward the most effective technique for pain reduction, improve ROM and decrease functional disability.
This Randomized Controlled Trial aims to effects of post-isometric relaxation (PIR) and active isolated stretch (AIS) techniques on reducing pain, improving range of motion, and decreasing functional disability in individuals with piriformis syndrome.
A Total of 40 participants will be recruited and randomized equally into two groups.
Both groups will additionally receive conventional management (TENs, Heating).
INTERVENTION SCHEDULE:
Group A (PIR): In this group, participant is asked to performed an isometric contraction in supine lying position with one leg crossed over the other, in which participant contracts the targeted muscle against resistance for about 6 to 10 seconds, followed by a relaxation phase of approximately 3 seconds Group B (AIS): In this group participant actively moves the limb to the end range of motion, followed by a brief, 1-2 second stretch applied by the therapist. Move the non-exercising leg across midline and rotate inward. The exercising leg is flexed at a 90° angle at the knee. Move the knee close to the opposite-side breast. Clasp the knee with the near hand and the top of the ankle with the far side hand. Rotate the thigh outward, moving the loot toward the surface with the far-side hand. This process is repeated for 8-10 repetitions.
ASSESSMENTS:
DATA ANALYSIS:
Intra-group comparisons (Pre vs Post) and Inter-group comparisons (PIR vs AIS) will be performed at the end of the 2-week intervention.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Group A - Post Isometric Relaxation | Active Comparator | Participants allocated to this arm will receive Post Isometric Relaxation. Each participant will undergo 6 sessions over 2 weeks (3 Sessions/week), and receive Conventional Physiotherapy |
|
| Group B - Active Isolated Stretch | Experimental | Participants allocated to this arm will receive Active Isolated Stretching. Each participant will undergo 6 sessions over 2 weeks (3 Sessions/week), and receive Conventional Physiotherapy |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Post Isometric Relaxation | Procedure | Participants allocated to this arm will receive Post Isometric Relaxation. Each participant will undergo 6 sessions over 2 weeks (3 Sessions/week), and receive Conventional Physiotherapy |
| Measure | Description | Time Frame |
|---|---|---|
| Pain Intensity | The Visual Analog Scale (VAS) will be used to measure the intensity of pain before and after the intervention. Participants will mark their level of pain on a 100 mm horizontal line, where: 0 mm indicates "no pain", and 100 mm indicates "the worst imaginable pain". | Before Treatment and after 2 weeks. |
| Range of Motion | A universal goniometer will be used to assess hip mobility in: Internal Rotation. ROM will be recorded in degrees. | Before treatment and after 2 weeks |
| Functional Disability | Oswestry Disability Index (ODI) It is used to measure functional disability. The Oswestry Disability Index (ODI) is one of the condition-specific questionnaires recommended for use with back pain patients. Interpretation: 0-20%: Minimal disability. 21-40%: Moderate disability. 41-60%: Severe disability (needs investigation). 61-80%: Crippled (needs active treatment). 81-100%: Bed-bound or exaggerating. | Before treatment and after 2 weeks |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Parsa Saghir, DPT | Contact | 0315-8962525 | parsa.saghir@gmail.com | |
| Muhammad Furqan Hassan, MS-OMPT | Contact | 0333-4056768 | furqan.hassan@fui.edu.pk |
| Name | Affiliation | Role |
|---|---|---|
| Parsa Saghir, DPT | Foundation University Islamabad | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Foundation University College of Physical Therapy | Recruiting | Islamabad | Punjab Province | 46000 | Pakistan |
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Participants will be randomly assigned into two parallel groups:
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| Active Isolated Stretching | Procedure | Participants allocated to this arm will receive Active Isolated Stretching. Each participant will undergo 6 sessions over 2 weeks (3 Sessions/week), and receive Conventional Physiotherapy. |
|
| ID | Term |
|---|---|
| D055958 | Piriformis Muscle Syndrome |
| D017116 | Low Back Pain |
| ID | Term |
|---|---|
| D020426 | Sciatic Neuropathy |
| D020422 | Mononeuropathies |
| D010523 | Peripheral Nervous System Diseases |
| D009468 | Neuromuscular Diseases |
| D009422 | Nervous System Diseases |
| D009408 | Nerve Compression Syndromes |
| D009437 | Neuralgia |
| D010146 | Pain |
| D009461 | Neurologic Manifestations |
| D012816 | Signs and Symptoms |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D017699 | Pelvic Pain |
| D001416 | Back Pain |
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