CClinicalTrials.gg
CompletedNCT02172079Updated Jun 24, 2014

Mobilization With Movement for Shoulder Impingement

An interventional study of Real mobilization-with-movement (MWM) and Sham mobilization-with-movement (MWM) in Shoulder Impingement Syndrome, sponsored by César Fernández-de-las-Peñas. Completed at 1 site in Spain. Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2014-06-24.

Sponsored by César Fernández-de-las-Peñas · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
42
Allocation
Randomized
Ages
18 Years to 65 Years
Sex
All
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Study summary

Controversy exists regarding the effectiveness of manual therapy techniques for the management of impingement syndrome. However, no adequately powered clinical trials have examined the effects of mobilization-with-movement. The purpose of the current study was to perform a randomized controlled trial comparing the effects of real MWM to a group receiving a sham intervention on shoulder pain at different moments and active shoulder range of motion in an adequately powered sample of patients with shoulder impingement syndrome.

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Conditions studied

  • Shoulder Impingement Syndrome

Keywords

  • shoulder impingement, manual therapy, pain, motion.
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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 42 is below the median of 54 across 261 interventional studies indexed under Shoulder Impingement Syndrome.

Browse Shoulder Impingement Syndrome studies →

Lead sponsor

César Fernández-de-las-Peñas is the lead sponsor of 5 studies on the registry; none are open to participants now.

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

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Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • history of shoulder pain of > 3months duration
  • pain localized at the proximal anterolateral shoulder region
  • medical diagnosis of shoulder impingement syndrome
  • at least 2 positive impingement tests including Neer, Hawking, or Jobe test

Exclusion criteria

Exclusion Criteria:

  • diagnosis of fibromyalgia
  • pregnancy
  • a history of traumatic onset of shoulder pain
  • other histories of shoulder injury
  • ligamentous laxity based on a positive Sulcus test and apprehension test
  • numbness or tingling in the upper extremity
  • previous shoulder or cervical spine surgery
  • corticosteroid injection on the shoulder within 1 year of the study
  • physical therapy 6 months prior to the study
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Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Outcomes assessor)
Enrollment
42 participants (actual)

Study arms

  • Experimental
    Real mobilization-with-movement (MWM)

    For the MWM group, an accessory posterior-lateral gliding movement in the humeral head combined with a movement of active shoulder flexion will be applied. One hand will be placed over the scapula posteriorly while the thenar eminence of the other hand will be placed over the anterior aspect of the head of the humerus

    Other: Real mobilization-with-movement (MWM)

  • Sham comparator
    Sham mobilization-with-movement (MWM)

    The sham condition will replicate the treatment condition except for the hand positioning. The therapist locates one hand over the belly of the pectoralis major muscle and the other over scapula without applying any pressure. The patient will be asked to move the arm in a similar manner as in the MWM group

    Other: Sham mobilization-with-movement (MWM)

Interventions

  • OtherReal mobilization-with-movement (MWM)
  • OtherSham mobilization-with-movement (MWM)
06

What researchers measure

Primary outcomes

  1. Changes in the intensity of shoulder pain before and after the treatment

    Participants were asked to rate the intensity of their pain using an 11-point numerical pain rating scale (NPRS; 0: no pain; 10: maximum pain) for 3 scores of perceived pain: 1, the intensity of shoulder pain experienced in the last 24h; 2, the intensity of shoulder pain at night; 3, the intensity of shoulder pain during shoulder flexion.

    Time frame: Baseline and one week after intervention

Secondary outcomes

  1. Changes in shoulder range of motion before and after the treatment

    A universal goniometer was used to assess the participant's shoulder range of motion in the following motions: * Pain-free and maximum (painful) range of motion in shoulder flexion * Pain-free range of motion in shoulder extension * Pain-free range of motion in shoulder abduction * Pain-free range of motion in shoulder external rotation * Pain-free range of motion in shoulder medial (internal) rotation

    Time frame: Baseline and one week after the intervention

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Study locations

1 site
  • Francisco Alburquerque Sendín
    Salamanca, 37008, Spain
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 24, 2014, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT02172079
Lead sponsor
César Fernández-de-las-Peñas
Collaborators
University of Salamanca
Responsible party
César Fernández-de-las-Peñas (Proffesor, Universidad Rey Juan Carlos) — Sponsor-investigator
First posted
Jun 24, 2014
Start date
Jan 2013
Primary completion
Jan 2014
Completion
Jan 2014
Last update
Jun 24, 2014

Study contacts

Francisco Alburquerque Sendín, PT, PhD
principal investigator · University of Salamanca
César Fernández de las Peñas, PT, PhD
study chair · Universidad Rey Juan Carlos

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jun 2014. You cannot join it, but the record below documents what was studied.

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