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Completed

NCT Number: NCT03883659

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

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.

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Key information

Age range

20 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Tri-Service General Hospital, Taipei, Neihu District, Taiwan

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About this study

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

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Smartphone

Other

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.

traditional paper hangouts

Other

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.

Primary outcomes

  1. home exercise adherence

    Time frame: 4 weeks

    the days patients do the home exercise program

Secondary outcomes

  1. shoulder range of motion

    Time frame: baseline, 4 weeks

    the mobility of shoulder

  2. Visual analog scale (VAS)

    Time frame: baseline, 4 weeks

    Ranged form 0 (minimum score) to 10 (Maximum score) ,the higher score represent more painful

  3. System usability scale (SUS)

    Time frame: 4 weeks

    the satisfaction scale of the smartphone program

Sponsors and collaborators

Lead sponsor

National Yang Ming Chiao Tung University

Other

Registry information

Important dates

Study start
2019
Primary completion
2019
Study completion
2019
First posted
Mar 21, 2019
Registry last updated
Aug 22, 2019

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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