ConditionShoulder Adhesive Capsulitis
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversity of Maryland, Baltimore
About this trial
The purpose of this study is to investigate the feasibility, usability and preliminary efficacy of a home-based Functional Electrical Stimulation(FES) in individuals with shoulder adhesive capsulitis. The main question it aims to answer is if combining home-based FES to usual therapy at the clinic will improve pain and improve function of the impaired shoulder.
Eligibility criteria
Qualifiers
Age > 18 years
Individuals diagnosed with shoulder adhesive capsulitis
Shoulder pain, limited shoulder mobility for more than 4 weeks, normal shoulder x-ray findings, and normal neurological exam
Can tolerate electrical stimulation
Disqualifiers
Presence of shoulder tumors or bone lesions
History of shoulder fracture or subluxation
History of shoulder surgery
Severe osteoporosis,
Trial design
Treatments tested in this trial
- Home based FES in combination with usual therapy
Treatment groups
10 Participants
are divided into 1 treatment groupSponsors and collaborators
Source ClinicalTrials.gov