Mode
Text Size
Log in / Sign up
N/A N=12 Treatment

Exercise Into Pain in Chronic Rotator Cuff Related Shoulder Pain: a Prospective Single-Group Feasibility Study

Shoulder Impingement Syndrome

Enrolled (actual)
12
Serious AEs
0.0%
Results posted
Jun 2025
Primary outcome: Primary: Rate of Adherence (Physiotherapy Session) — 7 Participants

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Exercise therapy (exercising into pain) (Other)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
Universiteit Antwerpen
Primary completion
May 2020

Outcome Measures

OutcomeResultp-value
PRIMARY
Rate of Adherence (Physiotherapy Session)
7
PRIMARY
Rate of Adherence (Adherence Home Exercises)
4
PRIMARY
Shoulder Pain and Disability Index (SPADI)
29.3
SECONDARY
Fear-Avoidance Beliefs Questionnaire (FABQ-PA)
1.5
SECONDARY
Fear-Avoidance Beliefs Questionnaire (FABQ-W)
3
SECONDARY
Fear of Pain Questionnaire (FPQ-9)
SECONDARY
Passive Range of Motion (ROM) in External Rotation
4
SECONDARY
Passive ROM in Internal Rotation
1
SECONDARY
Passive ROM in Scaption
27
SECONDARY
Active ROM in External Rotation
6
SECONDARY
Active ROM in Internal Rotation
-4
SECONDARY
Active ROM in Scaption
24
SECONDARY
Maximum Voluntary Contraction (MVC) in External Rotation
14.55
SECONDARY
MVC in Internal Rotation
26.64
SECONDARY
MVC in Scaption
6.54

Summary

The purpose of this study is to evaluate a) the feasibility of applying a painful exercise program in the treatment of subacromial shoulder pain and b) the time needed to collect clinical outcomes for a future randomized controlled trial.

Eligibility Criteria

Inclusion Criteria

  • Age 18-65 years
  • Shoulder pain for at least 3 months
  • Pain in the antero-lateral shoulder region
  • At least 3 out of 5 of the following tests positive: Neer test, Hawkins-Kennedy, Jobe, painful arc between 60° and 120°, external resistance test
  • Resting pain should be at 2/10 maximum on verbal NRS scale
  • All types of occupations were included: students, workers (including overhead workers or heavy duty workers), people on sick leave and retired people

Exclusion Criteria

  • Bilateral shoulder pain
  • Corticosteroid injections 6 weeks prior to the study
  • Pregnancy, inability to understand spoken or written Dutch
  • Clinical signs of full-thickness rotator cuff tears (positive external and internal rotation lag tests and drop arm test)
  • Evidence of adhesive capsulitis (50% or more than 30° loss of passive external rotation)
  • Previous cervical, thoracic or shoulder surgery; recent fractures or dislocations on the painful shoulder
  • Symptoms of cervical radiculopathy as primary complaint (tingling, radiating pain in the arm associated with neck complaints)
  • Primary diagnosis of acromioclavicular pathology, shoulder instability
  • A radiologically confirmed fracture or presence of calcification larger than 5 mm
  • Presence of competing pathologies (inflammatory arthritis, neurological disorders, fibromyalgia, malignancy)
  • More than 4h of training in sport overhead shoulder activities per week
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04154345). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

Back to search