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Piriformis SyndromeNCT07403045

McGill Strengthening With and Without Integrated Neuromuscular Inhibition Technique in Piriformis Syndrome

A study testing McGill strengthening exercises program, Integrated neuromuscular inhibition technique and Standardized physiotherapy treatment in people with Piriformis Syndrome, run by Riphah International University at 1 site in Pakistan.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The study was conducted to determine the effects of McGill strengthening exercises program with and without integrated neuromuscular inhibition technique on pain, range of motion and function in patients with piriformis syndrome. Read more about this study

Who is it for?
Ages 25 to 45 years
Conditions the study is for
Piriformis Syndrome
What is being tested?
McGill strengthening exercises program, Integrated neuromuscular inhibition technique and Standardized physiotherapy treatment
Could I receive a placebo?
No, everyone receives an active treatment
How many people
56 participants
Where
1 sitePakistan
Study dates
26 May 2025to 5 Nov 2025
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 25 to 45 years
  • All sexes
  • No healthy volunteers
  • Adult

Who may be able to join

  • Both genders with age ranged from 25 and 45 years
  • Sedentary
  • Non-traumatic
  • Idiopathic
  • External tenderness near the greater sciatic notch
  • Pain for more than 1 month's duration
Show all 13Show fewer
  • NPRS ranging from >3 to ≤ 6
  • Positive results on three of the following five tests:
  • FAIR
  • Beatty
  • Laségue
  • Pace
  • Freiberg

Who cannot join

  • Acute low back pain and/or acute lumbar radiculopathy
  • History of Stroke or any other neurological disorders
  • Recent buttock trauma
  • Inflammatory, infectious or tumor diseases
  • Severe vascular disease
  • Osteoporosis
  • Pregnancy

Trial locations and contacts

1 site in 1 country.

Pakistan1 site
  • Mumtaz Bakhtawar Memorial Trust Hospital, Mustafa Town

    Lahore, Punjab Province

Other trials in Pakistan

About this study

Official title: Effects of McGill Strengthening Exercises Program With and Without Integrated Neuromuscular Inhibition Technique on Pain, Range of Motion and Function in Patients With Piriformis Syndrome

The study was conducted to determine the effects of McGill strengthening exercises program with and without integrated neuromuscular inhibition technique on pain, range of motion and function in patients with piriformis syndrome.

Being tested
McGill strengthening exercises program, Integrated neuromuscular inhibition technique, Standardized physiotherapy treatment
Keywords
integrated neuromuscular inhibition technique, McGill exercises, pain, physical functional performance, piriformis syndrome, range of motion, trigger points
Medical subject headings
Piriformis Muscle Syndrome, Pain

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • McGill strengthening exercises programOther

    These exercises were divided into 3 phases, each lasting 2 weeks. Patients performed 4 repetitions of each exercise during 1st and 2nd week at each hospital visit. Then, increased by 4 repetitions every 2 weeks for up to 6 weeks. These exercises were performed with a maximum of 12 repetitions with a 1-minute of rest interval between each exercise. These exercises were performed by patients at each clinical visit, 3 days per week for total of 6 weeks.

  • Integrated neuromuscular inhibition techniqueOther

    This technique was applied at piriformis muscle. The procedure was repeated 3 times for up to 10 minutes at each clinical visit. This intervention was performed 3 days per week for total of 6 weeks.

  • Standardized physiotherapy treatmentOther

    These exercises were performed by patients at the end of each hospital visit (3 days per week for total of 6 weeks) and also at home twice a week during the 2 months follow-up period after treatment ends.

    1. Continuous-mode ultrasound therapy was applied at a frequency of 1 MHz and an intensity of 1.0 W/cm² for 3 minutes to the tender or trigger points on the posterior aspect of the pelvis.
    2. A hydrocollator pack (40°C) was applied for 10 minutes at lumbopelvic region.
    3. Piriformis, hamstring/calf stretching was performed progressively in phases.
    • Phase 1 consists of weeks 1 and 2 with 1 set of 3 repetitions with 30 seconds hold per day.
    • Phase 2 consists of weeks 3 and 4 with 2 sets of 3 repetitions with 30 seconds hold per day.
    • Phase 3 consists of weeks 5 and 6 with 2 sets of 3 repetitions with 30 seconds hold twice per day.
    • Follow-up period consists of 2 sets of 3 repetitions with 30 seconds hold twice per day.
Study groups in NCT07403045
Study groupRoleWhat they receive
McGill strengthening exercises program with integrated neuromuscular inhibition techniqueExperimentalNot described
Receives: Other: McGill strengthening exercises program; Other: Integrated neuromuscular inhibition technique; Other: Standardized physiotherapy treatment
McGill strengthening exercises programActive comparatorNot described
Receives: Other: McGill strengthening exercises program; Other: Standardized physiotherapy treatment

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Numeric Pain Rating Scale

    Numeric Pain Rating Scale (NPRS) was used to assess the patient's pain intensity. This scale ranges from 0 to 10, where 0 indicates "no pain" and 10 indicates "worst pain.

    Measured: From enrollment to 6 weeks of intervention with follow-up at 14 weeks.

Secondary outcomes (3)
  1. Range of Motion (Hip Abduction)

    The universal goniometer was used to assess hip abduction range of motion.

    Measured: From enrollment to 6 weeks of intervention with follow-up at 14 weeks.

  2. Range of Motion (Hip Internal Rotation)

    The universal goniometer was used to assess hip internal rotation range of motion.

    Measured: From enrollment to 6 weeks of intervention with follow-up at 14 weeks.

  3. Lower Extremity Functional Scale

    Lower Extremity Functional Scale was used to assess the patient's functional status. Maximum score of this scale is 80. The greater the score, the lower the disability.

    Measured: From enrollment to 6 weeks of intervention with follow-up at 14 weeks.

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted11 Feb 2026
  2. Study start26 May 2025
  3. Primary completion5 Sep 2025
  4. Study completion5 Nov 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Double blind
Who is masked
Participant, Outcomes assessor
Enrolment
56 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07403045
Sponsor's protocol ID
REC/RCR & AHS/24/0176
Status last verified
Feb 2026
First submitted
4 Feb 2026
Last updated
11 Feb 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Nazlikul H, Ural FG, Ozturk GT, Ozturk ADT. Evaluation of neural therapy effect in patients with piriformis syndrome. J Back Musculoskelet Rehabil. 2018;31(6):1105-1110. doi: 10.3233/BMR-170980.

    PubMed 30010101
  • Jamaly A, Mohsenifar H, Amiri A. The effects of dry needling in combination with physical therapy on improvement of pain and hip internal rotation range in patients with piriformis syndrome. Journal of Clinical Physiotherapy Research. 2018;3(3):118-22.

  • Awan WA, Babur MN, Ali S, Janjua U. The effectiveness of electrotherapy with manual therapy in the treatment of piriformis syndrome. Int J Rehabil Sci. 2018;1(1):16-9.

  • Laha K, Sarkar B, Kumar P, Patel L, Sarkar N. Efficacy of hip abductor and extensor strengthening on pain, strength and lower extremity function in piriformis syndrome: a randomized clinical trial. Int J Health Sci Res. 2018;8(9):80-.

  • Velappanchavadi C. Effectiveness of muscle energy technique versus stretching in subjects with piriformis syndrome. Int J Physiother Res. 2019;7(5):3252-56.

  • Alarab A, Unver F. Stretching exercise versus tissue mobilization technique in piriformis syndrome. European Journal of Medical and Health Sciences. 2020;2(6).

  • Kutty NN, Siddeeque S, Tamphaibema H, Othayoth N, Bineesh CP. Effect of Muscle Energy Technique with Deep Friction Massage on Pain, Disability and Internal Rotation Range of Motion of Hip Joint in Individuals with Piriformis Syndrome. Indian Journal of Physiotherapy & Occupational Therapy. 2020 Jan 1;14(1).

  • Athawale VK, Jethwani D, Qureshi MD, Dadgal R. Combined Effect of Neural Tissue Mobilization and Deep Friction Massage in Piriformis Syndrome: A Research Protocol. Indian Journal of Forensic Medicine & Toxicology. 2021 Apr 1;15(2).

  • Chaudhary S, Sheikh M, Chaudhary NI, Ambad R, Bankar N. Effect of neural tissue mobilization in combination with ultrasonic therapy verses ultrasonic therapy in deep gluteal syndrome-a comparative study.

  • RAZA H, ARSLAN HR, IQBAL A, HAMID MF, WASEEM A, MANZOOR S. Comparison Of Gluteal Muscle Strengthening Versus Conventional Isometrics In Pain Management Of Piriformis Syndrome. Age (years). 2021 Nov 1;50(5.79):45-31.

  • Roy S, Solanki N, Phd AC. Effectiveness of muscle energy technique versus static stretching in subject with tight piriformis in male office going subjects: a randomized clinical trial. IJRAR-International J Res Anal Rev. 2022;9(3):295-321.

  • Idrees KI, Khan KH, Sharif KH, Ahmad KH, Rahman HA, Fahad FA. Efficacy Of Hip Abductors Strengthening As Compared To Piriformis Muscle Stretching In Improving Lower Extremity Function In Patients With Piriformis Syndrome. Pakistan Journal of Medical & Health Sciences. 2022 Sep 16;16(07):721.

  • Ahmad N, Akram MJ, Hussain H, Imtiaz I, Khan N, Qi L. Effectiveness of post facilitation stretch technique versus myofascial release in piriformis syndrome: A Randomized controlled trial. Rawal Medical Journal. 2022 Nov 12;47(4):936.

  • Shahzadi B, Taj S, Nawaz S, Hamid I, Talpur MA, Hussain SA, Sajjad AG, Kiyani M. Sacroiliac joint manipulation helps to improve pain pressure threshold in chronic piriformis syndrome: a 6-week randomized controlled trial. The Rehabilitation Journal. 2023 Mar 31;7(01):476-82.

  • Ergezen G, Sahin M. Comparison of self-myofascial release and stretching exercises in individuals with piriformis syndrome: a randomised controlled trial. International Journal of Therapy And Rehabilitation. 2023 Nov 2;30(11):1-0.

Questions about this trial

What is this clinical trial studying?

A study testing McGill strengthening exercises program, Integrated neuromuscular inhibition technique and Standardized physiotherapy treatment in people with Piriformis Syndrome, run by Riphah International University at 1 site in Pakistan.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 13 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 11 Feb 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Pakistan. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Numeric Pain Rating Scale (time frame: From enrollment to 6 weeks of intervention with follow-up at 14 weeks.). It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT07403045, which also lists 23 linked publications.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 11 Feb 2026.

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