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A Pilot Study Comparing Two Rehabilitation Approaches for Individuals With Irritable Shoulder Pain

University of Central Florida logo

University of Central Florida

Status

Completed

Conditions

Shoulder Pain

Treatments

Other: Tissue Intervention
Other: Biopsychosocial Intervention

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

This pilot study will assess feasibility and obtain preliminary effects of a tissue based intervention to a biopsychosocial intervention in individuals with shoulder pain.

Enrollment

24 patients

Sex

All

Ages

18 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Shoulder pain intensity rated as 3/10 or higher in the past 24 hours

Exclusion criteria

  • Non-English speaking
  • Systemic medical conditions that affect sensation, such as uncontrolled diabetes
  • History of shoulder surgery or fracture within the past 6 months
  • blood clotting disorder, such as hemophilia
  • contraindication to the application of ice ((blood pressure > 140/90 mmHg, cold urticaria, cryogobulinemia, paroxysmal cold hemoglobinuria, circulatory compromise)
  • Unable to exercise without a medical clearance (assessed on the PAR-Q+ on the first visit)
  • Exceed pressure and sensory safety thresholds (assessed on the first visit)
  • Categorized as low irritability (assessed on the first visit)
  • currently pregnant
  • currently receiving physical therapy to treat shoulder pain

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

24 participants in 2 patient groups

Tissue Intervention
Experimental group
Description:
Participants will attend eight sessions. During each session, participants will receive education on positions of comfort, progressing activities, and return to function. Participants will complete shoulder stretching and strengthening exercises according to a protocol.
Treatment:
Other: Tissue Intervention
Biopsychosocial Intervention
Active Comparator group
Description:
Participants will attend eight sessions. During each session, participants will receive education on pain neuroscience education, stress management, and maintaining physical activity. Participants will complete shoulder stretching and strengthening exercises according to a graded exercise protocol.
Treatment:
Other: Biopsychosocial Intervention

Trial contacts and locations

1

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Central trial contact

Abigail Anderson

Data sourced from clinicaltrials.gov

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