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Subacute Effects of Spinal Mobilization to Treat Subacromial Impingement

Subacute Effects of Cervicothoracic Spinal Manipulation in Addition to Shoulder Manual Therapy Plus Exercise Intervention in Individuals With Subacromial Impingement Syndrome: a Randomized, Controlled Clinical Trial Pilot Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01753271
Enrollment
20
Registered
2012-12-20
Start date
2012-09-30
Completion date
Unknown
Last updated
2015-08-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Subacromial Impingement Syndrome

Brief summary

Specific Aims and Hypotheses Aims To investigate the incremental benefits of cervicothoracic spinal manipulation in addition to shoulder mobilization and exercise for improving range of motion, pain, physical function and fear avoidance beliefs in patients with subacromial shoulder impingement. Hypotheses It is hypothesized that those subjects who receive spinal manipulation in addition to shoulder mobilization and exercise will achieve greater improvements in range of motion, pain, function and fear avoidance beliefs at two weeks following treatment conclusion, at 4 weeks following treatment conclusion, and at discharge when compared to the subjects who did not receive the spinal manipulation.

Interventions

OTHERthoracic mobilization & shoulder mobilization & exercise
OTHERshoulder mobilization & exercise

Sponsors

University of Illinois at Chicago
CollaboratorOTHER
Walsh University
CollaboratorOTHER
High Point University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 50 Years
Healthy volunteers
No

Inclusion criteria

* To be eligible, participants must meet the clinical prediction rule for unilateral subacromial shoulder impingement including: a) positive Hawkins-Kennedy impingement sign, b) positive painful arc sign, and c) weakness in external rotation with the arm at the side

Exclusion criteria

* Individuals with contraindications to treatment with mobilization and manipulation (Appendix A) will be excluded

Design outcomes

Primary

MeasureTime frameDescription
Shoulder Pain and Disability Index Change over time2 weeks, 4 weeks, dischargePatients will be followed for the duration of their physical therapy treatment. An average of 12 visits over 6 weeks

Secondary

MeasureTime frameDescription
Numeric Pain Rating Scale change over time2 weeks, 4 weeks, dischargePatients will be followed for the duration of their physical therapy treatment. An average of 12 visits over 6 weeks
Fear Avoidance Beliefs Questionnaire change over time2 weeks, 4 weeks, dischargePatients will be followed for the duration of their physical therapy treatment. An average of 12 visits over 6 weeks

Other

MeasureTime frameDescription
Shoulder range of motion change over time2 weeks, 4 weeks, dischargePatients will be followed for the duration of their physical therapy treatment. An average of 12 visits over 6 weeks
test of resistance change over time - number of repetitions performed2 weeks, 4 weeks, dischargeThe test is performed by asking the patient to hold the shoulder at 90 degrees of shoulder flexion and follow a 20cm wide spiral using their affected arm. The patient is asked to complete as many spiral movements as possible until stopped secondary to pain. The maximum number of repetitions to be performed is 20. Patients will be followed for the duration of their physical therapy treatment. An average of 12 visits over 6 weeks

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 11, 2026