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Sports Physical TherapyNCT07062926

Comparative Effects of Spencer Muscle Energy Technique Versus Post Facilitation Stretch Among Fast Bowlers

A study testing Spencer Muscle Energy Technique and Post Facilitation Stretch in people with Sports Physical Therapy, run by Riphah International University at 1 site in Pakistan.

Not yet recruiting

Opening soon. The study is approved but enrolment has not started yet. Sites may already take enquiries.

Sites and contacts
Official record
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Trial summary

This study compares the effectiveness of Spencer Muscle Energy Technique and Post Facilitation Stretch in reducing shoulder pain in 32 fast bowlers aged 18-35. Participants will receive treatment three times a week for four weeks. Read more about this study

Who is it for?
Ages 18 to 35 yearsHealthy volunteers can take part
Conditions the study is for
Sports Physical Therapy
What is being tested?
Spencer Muscle Energy Technique and Post Facilitation Stretch
Could I receive a placebo?
No, everyone receives an active treatment
How many people
32 participants
Where
1 sitePakistan
Study dates
Jun 2026to 25 Aug 2026
Phase
Interventional
Are there results?
Not yet: the study is under way

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 18 to 35 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Fast bowlers
  • Both male and female.
  • aged 18-35 years.
  • Stiff painful shoulder joint for at least 3 months.
  • Willingness to participate in the study and provide informed consent.

Who cannot join

  • ● Rotator cuff tears.
  • Rheumatoid and gouty arthritis.
  • Tumors of the shoulder region.
  • Reflex sympathetic dystrophy of the shoulder.
  • Thoracic outlet syndrome, peripheral nerve injuries, shoulder girdle fractures, dislocations.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Muhammad Atif Javed, PP-DPT contact

03317491071

atif.javed@riphah.edu.pk

Syeda Tehreem Fatima, DPT contact

03311430000

temi.shah14@gmail.com

Pakistan1 site
  • Pakistan Sports Board

    Lahore, Punjab Province, 54000

Other trials in Pakistan

About this study

Official title: Comparative Effects of Spencer Muscle Energy Technique Versus Post Facilitation Stretch on Pain, Range of Motion, and Functional Disability Among Fast Bowlers With Shoulder Pain

This study compares the effectiveness of Spencer Muscle Energy Technique and Post Facilitation Stretch in reducing shoulder pain in 32 fast bowlers aged 18-35. Participants will receive treatment three times a week for four weeks. Pain, shoulder mobility, and functional ability will be measured before and after the intervention to identify the more effective technique

Read the detailed description

This randomized clinical trial aims to compare the effectiveness of the Spencer Muscle Energy Technique and Post Facilitation Stretch in treating shoulder pain among fast bowlers. A total of 32 fast bowlers aged 18-35 years with chronic shoulder pain will be recruited from the Pakistan Sports Board, Lahore. Participants will be randomly divided into two groups, each receiving one of the two treatments three times a week for four weeks, preceded by hot pack application. Pain, shoulder range of motion, and functional disability will be assessed before and after the intervention using the Visual Analogue Scale, inclinometer, and Quick-DASH questionnaire. The study seeks to determine which technique offers better outcomes for managing shoulder pain in fast bowlers.

Being tested
Spencer Muscle Energy Technique, Post Facilitation Stretch
Keywords
spencer technique, post facilitation stretch, shoulder pain.
Medical subject headings
Shoulder Pain

What participants receive

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

  • Spencer Muscle Energy TechniqueOther

    Also called Assigned

    Spencer muscle energy technique participants will receive a hot pack for 7-10 minutes followed by their respective treatments, three times a week for four weeks. Group A will undergo Spencer Muscle Energy Technique for 30 minutes

  • Post Facilitation StretchOther

    Also called Assigned

    Post facilitation stretch participants will receive a hot pack for 7-10 minutes followed by their respective treatments, three times a week for four weeks.post facilitation stretching process was repeated 5 times with 10 second interval between each stretch.

Study groups in NCT07062926
Study groupRoleWhat they receive
Spencer Muscle Energy TechniqueExperimental16 participants will undergo spencer muscle energy technique three times a week over a four-week period.Various movement patterns will performed, and the treatment duration will be 30 minutes.
Receives: Other: Spencer Muscle Energy Technique
Post Facilitation StretchExperimental16 participants will undergo Post facilitation stretching process was repeated 5 times with 10 second interval between each stretch. The whole treatment session was around 20 minute.
Receives: Other: Post Facilitation Stretch

What is being measured

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

  1. Visual Analogue Scale

    Pain intensity was measured using a 10-cm VAS, where 0 indicates "no pain" and 10 indicates "worst imaginable pain." Scores were recorded at baseline and after 4 weeks of intervention.

    Measured: 4 Weeks

  2. Range of Motion

    Active shoulder flexion, abduction, and external rotation were assessed using a digital inclinometer. Each movement was measured three times and averaged. Assessments were conducted at baseline and after the intervention period.

    Measured: 4 Weeks

  3. Quick Disabilities of the Arm, Shoulder and Hand (Quick-DASH) Score

    A validated questionnaire used to assess functional disability of the upper limb. It consists of 11 items scored on a 5-point Likert scale. Final scores range from 0 (no disability) to 100 (most severe disability). It was recorded pre- and post-intervention.

    Measured: 4 Weeks

Timeline

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

  1. First posted14 Jul 2025
  2. Study startJun 2026 (estimated)
  3. Primary completion20 Aug 2026 (estimated)
  4. Study completion25 Aug 2026 (estimated)

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
Model description
Randomized control design
Masking
Single blind
Who is masked
Participant
Enrolment
32 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07062926
Sponsor's protocol ID
REC/RCR&AHS/24/0447
Status last verified
Jun 2026
First submitted
3 Jul 2025
Last updated
10 Jun 2026
Results posted
No
Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Publications

  • Ghisi D, Boschetto G, Spinelli AM, Giannone S, Frugiuele J, Ciccarello M, Bonarelli S. Spinal anaesthesia with Chloroprocaine HCl 1% for elective lower limb procedures of short duration: a prospective, randomised, observer-blind study in adult patients. BMC Anesthesiol. 2021 Feb 20;21(1):58. doi: 10.1186/s12871-021-01279-9.

    PubMed 33610175
  • Kawabata Y, Ikegami H. Genetics of fulminant type 1 diabetes. Diabetol Int. 2020 Sep 21;11(4):315-322. doi: 10.1007/s13340-020-00468-0. eCollection 2020 Oct.

    PubMed 33088637
  • Su PY, Su WW, Hsu YC, Wang SY, Chiu PF, Yen HH. Micro-Elimination of Hepatitis C among Patients with Kidney Disease by Using Electronic Reminder System-A Hospital-Based Experience. J Clin Med. 2022 Jan 14;11(2):423. doi: 10.3390/jcm11020423.

    PubMed 35054120
  • Chia M. PRIDE for PLAY: Personal Responsibility in Daily Effort for Participation in Lifelong Activity for Youths. A Singaporean Context. J Sports Sci Med. 2007 Sep 1;6(3):374-9.

    PubMed 24149424
  • Phansopkar P, Qureshi MI. Impact of Spencer Technique on Pain, Range of Motion, and Functional Disability in Patients With Frozen Shoulder: A Pilot Study. Cureus. 2024 Jan 30;16(1):e53263. doi: 10.7759/cureus.53263. eCollection 2024 Jan.

    PubMed 38435910
  • Iqbal M, Riaz H, Ghous M, Masood K. Comparison of Spencer muscle energy technique and Passive stretching in adhesive capsulitis: A single blind randomized control trial. J Pak Med Assoc. 2020 Dec;70(12(A)):2113-2118. doi: 10.5455/JPMA.23971.

    PubMed 33475581

Questions about this trial

What is this clinical trial studying?

A study testing Spencer Muscle Energy Technique and Post Facilitation Stretch in people with Sports Physical Therapy, 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 5 inclusion and 5 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: opening soon, as of the sponsor's last update on 10 Jun 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?

This study is still under way. Results are not available in the source record yet.

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

Contact Muhammad Atif Javed, PP-DPT (03317491071, atif.javed@riphah.edu.pk), or a site near the patient. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Visual Analogue Scale (time frame: 4 Weeks). The study lists 3 primary outcomes in all. 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 NCT07062926, which also lists 6 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 10 Jun 2026.

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