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Smartphone-based Mobility Assessment and Individualized Exercise Programs for Patients With Frozen Shoulder

Smartphone-based Mobility Assessment and Individualized Exercise Programs for Patients With Frozen Shoulder

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03883659
Enrollment
11
Registered
2019-03-21
Start date
2019-04-01
Completion date
2019-07-30
Last updated
2019-08-22

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

Conditions

Frozen Shoulder

Keywords

frozen shoulder, smartphone, home exercise program, range of motion

Brief summary

This study was to investigate the reliability and validity of the smartphone goniometer app to measure shoulder ROM in a modified position for patients with frozen shoulder, and compare the intervention effect and adherence to home exercise between the smartphone and traditional paper hangouts.

Detailed description

This study was to investigate the reliability and validity of the smartphone goniometer app to measure shoulder ROM in a modified position for patients with frozen shoulder, and compare the intervention effect and adherence to home exercise between the smartphone and traditional paper hangouts. The outcome measure including shoulder range of motion, pain condition, home exercise adherence and satisfaction of smartphone program

Interventions

OTHERSmartphone

patients with frozen shoulder in the smartphone group will use the smartphone to conduct the home exercise program. The patients will be asked to follow the description to have mobility assessment at least 1 week and do the individualized exercise themselves.

OTHERtraditional paper hangouts

patients with frozen shoulder in the smartphone group will use the paper hangouts to conduct the home exercise program. The content of the paper hangouts were description of the home exercise.

Sponsors

National Yang Ming Chiao Tung University
Lead SponsorOTHER

Study design

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

Masking description

one assessor who don't know the group will measure the range of motion by using goniometer

Intervention model description

randomized controlled trial

Eligibility

Sex/Gender
ALL
Age
20 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

* gradual shoulder pain and stiffness at least 4 months * loss of active and passive shoulder mobility, shoulder external rotation \<45 degree * ability to use the smartphone

Exclusion criteria

* normal shoulder mobility * diagnostic shoulder osteoarthritis * nerve pain * injection of corticosteroids in 3 months

Design outcomes

Primary

MeasureTime frameDescription
home exercise adherence4 weeksthe days patients do the home exercise program

Secondary

MeasureTime frameDescription
shoulder range of motionbaseline, 4 weeksthe mobility of shoulder
Visual analog scale (VAS)baseline, 4 weeksRanged form 0 (minimum score) to 10 (Maximum score) ,the higher score represent more painful
System usability scale (SUS)4 weeksthe satisfaction scale of the smartphone program

Countries

Taiwan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026