CClinicalTrials.gg
CompletedNCT07458711Updated Mar 9, 2026

Comparative Effects of Spencer Techniques and Movement With Mobilization in Improving Pain, Range of Motion, and Functional Disability in Rotator Cuff Syndrome.

An interventional study of Spencer technique and Movement with mobilization in Rotator Cuff Syndrome, sponsored by University of Lahore. Completed at 1 site in Pakistan. Open to participants aged 30 Years to 60 Years. Per ClinicalTrials.gov, last updated 2026-03-09.

Sponsored by University of Lahore · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 5 months after the study started (first participant enrolled Sep 2025, registered Mar 2026).
Phase
Not applicable
Study type
Interventional
Enrollment
60
Allocation
Randomized
Ages
30 Years to 60 Years
Sex
All
01

Study summary

This study will be randomised clinical trial conducted at the University of Lahore Teaching Hospital, Lahore, Pakistan. A total of 60 participants will be selected and randomly allocated into two treatment groups (30 participants in each group) using the lottery method. All screened and willing participants who meet the eligibility criteria will be assigned to either Group A or Group B. Group A: Spencer Technique with Conventional Therapy

Participants allocated to Group A will receive the Spencer Technique in combination with conventional physiotherapy. The intervention will follow a structured and progressive protocol for 6 weeks.

Conventional Therapy (15 minutes per session)

Conventional treatment will be administered prior to manual therapy and will include:

Moist Hot Pack (5 minutes):

A moist hot pack will be applied to the affected shoulder at a comfortable therapeutic temperature. A towel layer will be placed between the hot pack and the skin to prevent burns.

Shoulder Stretching Exercises (10 minutes):

Passive stretching will be performed to improve flexibility, reduce muscle tightness, and enhance shoulder range of motion. Each stretch will be held for 20-30 seconds and repeated 3-5 times. Stretching will include:

Shoulder flexion and extension (supine position)

Shoulder abduction

Shoulder adduction (cross-body stretch)

Internal and external rotation at 90° abduction

Stretching will be performed five sessions per week.

Spencer Technique (20 minutes per session)

Following conventional therapy, the Spencer technique will be administered in seven sequential steps:

Shoulder extension with elbow flexion to the point of restriction

Shoulder flexion with elbow extension

Circumduction with compression at 90° abduction

Circumduction with distraction at 90° abduction

Abduction with internal rotation (hand placed behind hip)

Adduction with external rotation

Stretching with fluid pumping maneuver (5-10 repetitions)

Dosage and Progression:

Frequency: 5 sessions per week

Weeks 1-3: 2 sets of 10 repetitions per step (1-minute rest between sets)

Weeks 4-6: 3 sets of 10 repetitions per step

Total session duration: 35 minutes

5 minutes hot pack

10 minutes stretching

20 minutes Spencer technique

Group B: Mobilization with Movement (MWM) with Conventional Therapy

Participants allocated to Group B will receive Mobilization with Movement combined with conventional physiotherapy for 6 weeks.

Conventional Therapy (15 minutes per session)

The same conventional therapy protocol as Group A will be administered prior to mobilization:

5 minutes moist hot pack

10 minutes passive shoulder stretching

Mobilization with Movement (20 minutes per session)

MWM will be performed in the directions of:

External rotation

Internal rotation

Abduction

Flexion

The participant will be positioned in sitting on a high chair. The therapist will stabilize the shoulder girdle with one hand while applying a sustained glide to the humeral head using the thenar eminence of the other hand. The glide will be maintained perpendicular to the plane of movement and adjusted according to the participant's pain-free direction.

Participants will be instructed to actively move the shoulder through the available range while the glide is sustained. Movement will continue until the onset of pain or discomfort.

Dosage:

3 sets of 10 repetitions

30-second rest between sets

Frequency: 3 sessions per week

Duration: 6 weeks

Total session duration: 35 minutes

5 minutes hot pack

10 minutes stretching

20 minutes mobilization with movement

Read the detailed description

Study Design and Procedures

This study is a single-blinded, randomized controlled trial designed to compare the effectiveness of the Spencer Technique combined with conventional therapy versus Mobilization with Movement combined with conventional therapy in individuals with shoulder dysfunction.

Screening and Recruitment

Participants who meet the predefined inclusion criteria will be recruited using a purposive sampling technique. Individuals who are readily available and willing to participate will be screened for eligibility.

Eligible participants will be informed about the study objectives, procedures, potential risks, and benefits. Written informed consent will be obtained prior to enrollment.

Sample Size and Allocation

A total sample of 52 participants will be included in the study. After baseline assessment, participants will be randomly allocated into two groups (Group A and Group B) using the lottery method.

Randomization

Randomization will be performed using a simple lottery method to ensure equal allocation into the two intervention groups.

Blinding

This study will follow a single-blinded design. Participants will be blinded to group allocation.

Intervention Duration and Assessment

Both groups will receive treatment for 6 weeks. Sessions will be conducted 3 times per week. Outcome assessments will be performed at baseline and at the end of the 6th week.

Each treatment session for both groups will have a total duration of 35 minutes.

Data will be analyzed using Statistical Package for the Social Sciences (SPSS) version 27.0.

Interventions Group A: Spencer Technique with Conventional Therapy

Participants allocated to Group A will receive the Spencer Technique in combination with conventional physiotherapy.

Conventional Therapy (15 minutes per session)

Moist Hot Pack (5 minutes):

A moist hot pack will be applied to the affected shoulder at a therapeutic temperature, with a towel placed between the pack and the skin.

Shoulder Stretching (10 minutes):

Passive stretching exercises will be performed to improve flexibility and range of motion. Each stretch will be held for 20-30 seconds and repeated 3-5 times. Stretching will include:

Shoulder flexion and extension

Shoulder abduction

Shoulder adduction

Internal and external rotation at 90° abduction

Spencer Technique (20 minutes per session)

The technique will be administered in seven sequential steps:

Shoulder extension with elbow flexion to restriction

Shoulder flexion with elbow extension

Circumduction with compression at 90° abduction

Circumduction with distraction at 90° abduction

Abduction with internal rotation

Adduction with external rotation

Stretching with fluid pumping maneuver (5-10 repetitions)

Dosage progression:

Weeks 1-3: 2 sets of 10 repetitions per step (1-minute rest between sets)

Weeks 4-6: 3 sets of 10 repetitions per step

Total session duration: 35 minutes (5 minutes hot pack, 10 minutes stretching, 20 minutes Spencer technique).

Group B: Mobilization with Movement with Conventional Therapy

Participants allocated to Group B will receive Mobilization with Movement (MWM) combined with conventional physiotherapy.

Conventional Therapy (15 minutes per session)

5 minutes moist hot pack

10 minutes passive shoulder stretching

Mobilization with Movement (20 minutes per session)

Participants will be positioned in sitting. The therapist will stabilize the shoulder girdle with one hand and apply a sustained glide to the humeral head using the thenar eminence of the other hand. The glide will be maintained perpendicular to the plane of movement and adjusted to remain pain-free.

Mobilization will be performed in:

External rotation

Internal rotation

Abduction

Flexion

Participants will actively move the shoulder during sustained glide until the onset of pain or discomfort.

Dosage:

3 sets of 10 repetitions

30-second rest between sets

3 sessions per week for 6 weeks

Total session duration: 35 minutes (5 minutes hot pack, 10 minutes stretching, 20 minutes mobilization).

02

Conditions studied

  • Rotator Cuff Syndrome

Keywords

  • rotator cuff impingement or syndrome
03

In context

Shoulder Impingement Syndrome

304 studies on the registry are indexed under Shoulder Impingement Syndrome; 55 are open to participants now.

This study's enrollment of 60 is above the median of 54 across 261 interventional studies indexed under Shoulder Impingement Syndrome.

Browse Shoulder Impingement Syndrome studies →

Lead sponsor

University of Lahore is the lead sponsor of 223 studies on the registry; 40 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
30 Years to 60 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

    • Patient from the age of 30 to 60.

      • Patient suffering from rotator cuff syndrome. Patient with a history of pain in shoulder for more than 3 month.
      • Patient with grade 1 and grade 2 of rotator cuff syndrome which doesn't require surgery.
      • Patient with 2 positive Neers and Hawkins Kennedy test.
      • Patient who haven't gone under any physical therapy treatment in the past 6 months.

Exclusion criteria

Exclusion Criteria:

    • Patient with any cardiac problem like myocardial infarction.

      • Patient with diagnosis of fibromyalgia.
      • Patient with ongoing pregnancy.
      • Patient with pain related to shoulder trauma.
      • Patient with history of shoulder injury or shoulder surgery.
      • Patient with associated symptoms like numbness and tingling.
      • Patient who have taken corticosteroids injections of shoulder within a year.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
60 participants (actual)

Study arms

  • Experimental
    Spencer technique + conventional physical therapy

    The technique will be administered in seven sequential steps: Shoulder extension with elbow flexion to restriction Shoulder flexion with elbow extension Circumduction with compression at 90° abduction Circumduction with distraction at 90° abduction Abduction with internal rotation Adduction with external rotation Stretching with fluid pumping maneuver (5-10 repetitions) Dosage progression: Weeks 1-3: 2 sets of 10 repetitions per step (1-minute rest between sets) Weeks 4-6: 3 sets of 10 repetitions per step Total session duration: 35 minutes (5 minutes hot pack, 10 minutes stretching, 20 minutes Spencer technique).

    Other: Spencer technique · Other: conventional physical therapy

  • Experimental
    movement with mobilization + conventional physical therapy

    The technique will be administered in seven sequential steps: Shoulder extension with elbow flexion to restriction Shoulder flexion with elbow extension Circumduction with compression at 90° abduction Circumduction with distraction at 90° abduction Abduction with internal rotation Adduction with external rotation Stretching with fluid pumping maneuver (5-10 repetitions) Dosage progression: Weeks 1-3: 2 sets of 10 repetitions per step (1-minute rest between sets) Weeks 4-6: 3 sets of 10 repetitions per step Total session duration: 35 minutes (5 minutes hot pack, 10 minutes stretching, 20 minutes Spencer technique).

    Other: Movement with mobilization · Other: conventional physical therapy

Interventions

  • OtherSpencer technique

    Spencer Technique (20 minutes per session) The technique will be administered in seven sequential steps: Shoulder extension with elbow flexion to restriction Shoulder flexion with elbow extension Circumduction with compression at 90° abduction Circumduction with distraction at 90° abduction Abduction with internal rotation Adduction with external rotation Stretching with fluid pumping maneuver (5-10 repetitions) Weeks 1-3: 2 sets of 10 repetitions per step (1-minute rest between sets) Weeks 4-6: 3 sets of 10 repetitions per step

  • OtherMovement with mobilization

    Mobilization will be performed in: External rotation Internal rotation Abduction Flexion Participants will actively move the shoulder during sustained glide until the onset of pain or discomfort. Dosage: 3 sets of 10 repetitions 30-second rest between sets 3 sessions per week for 6 weeks Conventional Therapy (15 minutes per session) Moist Hot Pack (5 minutes): A moist hot pack will be applied to the affected shoulder at a therapeutic temperature, with a towel placed between the pack and the skin. Shoulder Stretching (10 minutes): Passive stretching exercises will be performed to improve flexibility and range of motion. Each stretch will be held for 20-30 seconds and repeated 3-5 times. Stretching will include: Shoulder flexion and extension Shoulder abduction Shoulder adduction Internal and external rotation at 90° abduction Total session duration: 35 minutes (5 minutes hot pack, 10 minutes stretching, 20 minutes mobilization).

  • Otherconventional physical therapy

    Conventional Therapy (15 minutes per session) Moist Hot Pack (5 minutes): A moist hot pack will be applied to the affected shoulder at a therapeutic temperature, with a towel placed between the pack and the skin. Shoulder Stretching (10 minutes): Passive stretching exercises will be performed to improve flexibility and range of motion. Each stretch will be held for 20-30 seconds and repeated 3-5 times. Stretching will include: Shoulder flexion and extension Shoulder abduction Shoulder adduction Internal and external rotation at 90° abduction

06

What researchers measure

Primary outcomes

  1. Pain Intensity (Visual Analogue Scale)

    Visual Analogue Scale The Visual Analogue Scale (VAS) is a subjective measure in which individuals rate their pain on an eleven-point numerical scale. The scale is composed of 0 (no pain at all) to 10 (worst imaginable pain). According to researches VAS shows excellent reliability (0.97 and 0.99, respectively) for the measurement of musculoskeletal pain.

    Time frame: baseline, 3rd week , 6th week

Secondary outcomes

  1. range of motion

    Goniometer Range of motion is measured using a goniometer at baseline and end point measurements. Range of motion of joints are usually assessed by a device known as universal goniometer. goniometer has two arms stationary as well as movable arm. The centre of the goniometer is known as fulcrum. Through goniometer in each plane joint ranges are measured. Goniometer Positioning for Shoulder Joint Assessment For Goniometer assessment fulcrum with be place on the shoulder joint. On the other hand it was in aligned with frontal axis in terms of assessing flexion and extension and add sagittal axis in terms of assessing abduction and abduction and in longitudinal axis for internal and external rotation.

    Time frame: baseline, 3rd week, 6th week

  2. for function (DASH)

    Disability of Arm, Shoulder, and Hand (DASH) questionnaire The Disability of Arm, Shoulder, and Hand (DASH) questionnaire consists of 30 items designed to evaluate self-reported disability. It measures both symptoms and physical abilities related to upper musculoskeletal conditions. Additionally, it assesses upper limb impairment by tracking changes in symptoms and functionality over time. The questionnaire demonstrates strong reliability (0.96) and solid validity (0.70).

    Time frame: Baseline, 3rd week, 6th week

07

Study locations

1 site
  • University of Lahore Teaching Hospital
    Lahore, Punjab Province 55150, Pakistan
08

References and documents

Individual participant data

Plan to share: No

No publications or documents are linked to this record.

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 9, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07458711
Lead sponsor
University of Lahore
Collaborators
University of Lahore Hospital (ULH)
Responsible party
Sponsor
First posted
Mar 9, 2026
Start date
Sep 26, 2025
Primary completion
Feb 28, 2026
Completion
Mar 3, 2026
Last update
Mar 9, 2026

Study contacts

Asim Arif, PhD scholar
principal investigator · University of Lahore

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Sep 2025. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion