CClinicalTrials.gg
CompletedNCT02374073Updated Feb 27, 2015

Functional Massage of Teres Major Muscle

An interventional study of Functional Massage and Protocolized physiotherapy in Subacromial Impingement Syndrome and Trigger Points, sponsored by Fundacio d'Investigacio en Atencio Primaria Jordi Gol i Gurina. Completed. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2015-02-27.

Sponsored by Fundacio d'Investigacio en Atencio Primaria Jordi Gol i Gurina · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
58
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

Purpose: Subacromial impingement syndrome is the most common shoulder condition. Myofascial trigger points in teres major muscle can be associated with this syndrome. The investigators objective is to find out if adding manual therapy specifically for teres major trigger points can produce better results in these patients.

Method: A randomized controlled pilot study was carried out. Fifty people were randomly assigned to one of two groups: intervention group or control group. Both groups received a protocolized physical therapy treatment while the intervention group additionally received manual therapy for teres major trigger points.

02

Conditions studied

  • Subacromial Impingement Syndrome
  • Trigger Points
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 58 is close to the median of 54 across 261 interventional studies indexed under Shoulder Impingement Syndrome.

Browse Shoulder Impingement Syndrome studies →

Lead sponsor

Fundacio d'Investigacio en Atencio Primaria Jordi Gol i Gurina is the lead sponsor of 158 studies on the registry; 20 are open to participants now.

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

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • Age 18 years and over
  • Clinical diagnosis of Subacromial Impingement Syndrome.
  • Detectable trigger points in teres major muscle.
  • Sign informed consent form.

Exclusion criteria

Exclusion Criteria:

  • Presence of wounds or cutaneous alterations in the shoulder region
  • Previous surgery in the shoulder
  • Presence of acute inflammatory process in the shoulder (\< 7 days),
  • Being involved in litigation or compensation processes
  • Not having a domain of the language that could make the informed consent not understandable.
05

Study design

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

Study arms

  • Experimental
    Intervention group

    Treated with protocolized physiotherapy and functional massage

    Other: Functional Massage · Other: Protocolized physiotherapy

  • Experimental
    Control group

    Treated with protocolized physiotherapy

    Other: Protocolized physiotherapy

Interventions

  • OtherFunctional Massage

    The functional massage is a manual therapy technique, indicated in cases of painful muscle tightness that combines a rhythmical and non painful passive joint mobilization in the direction of muscle stretching together with compression/decompression of the muscle to be treated.

  • OtherProtocolized physiotherapy

    therapeutic exercises, analgesic electrotherapy and cryotherapy

06

What researchers measure

Primary outcomes

  1. Change in Pain Intensity (visual analogue scale)

    Using a Visual analogue scale

    Time frame: Change from baseline to 3 weeks

Secondary outcomes

  1. Change in Function (Abbreviated Constant-Murley score)

    Using the Abbreviated Constant-Murley score

    Time frame: Change from baseline to 3 weeks

  2. Change in Active Range of Motion

    Flexion, extension, abduction, external rotation and internal rotation

    Time frame: Change from baseline to 3 weeks

07

Study locations

No study locations are listed for this record.

08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Feb 27, 2015, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT02374073
Lead sponsor
Fundacio d'Investigacio en Atencio Primaria Jordi Gol i Gurina
Responsible party
Sponsor
First posted
Feb 27, 2015
Start date
Jan 2014
Primary completion
Mar 2014
Completion
Mar 2014
Last update
Feb 27, 2015

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Feb 2015. 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