Rotator Cuff Tendinitis
Conditions
Keywords
isometric exercise, rotator cuff, pain threshold
Brief summary
The aim of this study is to compare the immediate effects of an acute bout of isometric exercise of the shoulder external rotator muscles above and below pain threshold on pain intensity, pain threshold, conditioned pain modulation and pain free force in external rotation. To evaluate the results of the exercise, the subjects will be assessed at pre-intervention, immediately post-intervention and after and 45 minutes after each experimental condition.
Detailed description
The aim of this study is to compare the immediate effects of an acute bout of isometric exercise of the shoulder external rotator muscles above and below pain threshold on pain intensity, pain threshold, conditioned pain modulation and pain free force in external rotation. It will consist of a randomized three-treatment parallel-design study. The sample will consist of subjects with rotator cuff related shoulder pain (RCRSP). Once the sample is selected, subjects will participate in three experimental sessions, which will occur in a randomized order: two exercise sessions (supra-threshold and infra-threshold isometric exercise) and one control session. In the first session, information regarding clinical and demographical aspects will be collected. A washout period of approximately 48 hours will separate each of the experimental sessions. To evaluate the results of the exercise, the subjects will be assessed at pre-intervention, immediately post-intervention and 45 minutes after each experimental condition. Pain intensity, Pressure Pain Thresholds (PPT), Conditioned Pain Modulation (CPM), maximal voluntary isometric contraction (MVIC) and pain free isometric strength (PFIS) will be measured.
Interventions
OTHERSupra-threshold isometric exercise
The supra-threshold intensity will be stablished at 120% of participant's PFIS pre-session measurement (20% above the individual's pain threshold).
OTHERInfra-threshold isometric exercise
The infra-threshold intensity will be stablished at 80% of participant's PFIS pre-session measurement (20% bellow the individual's pain threshold).
Sponsors
University of Valencia
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Investigator)
Masking description
Exercise sessions were delivered by a physiotherapist who was not involved in the assessments.
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* aged 18-80 years (likelihood of patients \> 80 having degenerative changes in the shoulder is increased) * pain localised to the proximal anterolateral shoulder region * positive for pain on at least one of the following three impingement tests: Hawkins-Kennedy, Neer's, Jobe's * positive for pain on resisted external rotation and/or abduction.
Exclusion criteria
* shoulder surgery within last 6 months * reasons to suspect systemic pathology including inflammatory disorders, cervical repeated movement testing affects shoulder pain and/or range of movement, passive external rotation deficit greater (less than 30º or a range of motion reduction of 50% or more as compared to the contralateral side), upper limb tension test A for cervical radiculopathy * atraumatic degenerative rotator cuff tear based on the cluster of clinical tests (painful arc, drop arm test, and marked weakness into ER all three positive)
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Pain intensity | Baseline | Shoulder pain intensity reported by the patient will be assessed using a 100-mm visual analogue scale (VAS, 0-100, 0=minimum score, 100=maximum score). Higher values represent a better outcome (less pain). |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Pressure Pain Thresholds (PPT) | Baseline, immediately post-intervention and 45 minutes post-intervention | PPTs will be recorded using an electronic algometer at the ipsilateral m. infraspinatus, the contralateral resting m. infraspinatus and the contralateral resting m. quadriceps. Higher values represent a better outcome. |
| Conditioned pain modulation (CPM) | Baseline | CPM will be tested using the upper extremity submaximal effort tourniquet test. |
| Maximal voluntary isometric contraction (MVIC) | Baseline | MVIC will be measured at both m. infraspinatus and m. quadriceps of the non-affected side using a digital force gauge. |
| Pain free isometric strength/threshold (PFIS) | Baseline | PFIS will be assessed at m. infraspinatus of the affected shoulder |
Countries
Spain
Outcome results
None listed