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CompletedNCT02135978Updated Apr 11, 2018

Maintenance of Shoulder Health and Function After Spinal Cord Injury

An interventional study of Shoulder home exercise program in Spinal Cord Injury and Shoulder Pain, sponsored by Rancho Research Institute, Inc.. Completed at 1 site in United States. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2018-04-11.

Sponsored by Rancho Research Institute, Inc. · Not applicable, Interventional, and Prevention

Phase
Not applicable
Study type
Interventional
Enrollment
148
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

The purpose of this study is to determine if a shoulder exercise program can prevent the onset of shoulder pain and improve community participation in persons who have a spinal cord injury (SCI). Upon entry into the study patients will have pain-free shoulders and will be followed for 3 years to determine rate of shoulder pain development. Patients will learn a simple shoulder home exercise program and will be instructed on techniques to protect their shoulder during wheelchair propulsion, transfers and activities of daily living. Patients will be instructed to perform the home exercise program 3 days per week. Two types of treatment (training) delivery approaches that have been documented to reduce chronic shoulder pain will be compared. The rate of shoulder pain development for the two groups will be compared to the rate of shoulder pain development in the historical control group. The investigators hypothesize that the rate of shoulder pain development will be lower in the experimental treatment groups compared to the historical control group. Any differences between the two treatment delivery approaches for the experimental treatment groups will help to provide guidelines for the most effective delivery approach of a shoulder pain prevention program.

Read the detailed description

All persons are at risk for shoulder pain from a shoulder injury or rotator cuff injury. Persons with SCI are at a greater risk because of the increased use of their shoulders. Lifestyle changes following SCI place a large demand on an individual's shoulders. Pushing a wheelchair, transferring, and performing pressure relief raises are three common activities that put added strain on the shoulders. In addition to these activities, reaching from a wheelchair can put strain on the shoulder because many environments are not ideally set up for wheelchair users. These new stressors are believed by the medical community to lead to shoulder pain. The prevalence of shoulder pain for persons with spinal cord injury is 30-70%. Untreated, shoulder pain may lead to additional losses in function and community mobility.

Previous research shows that shoulder exercises along with education on how to improve one's technique for wheelchair propulsion, transfers, and weight relief raises can significantly reduce chronic shoulder pain and improve quality of life. The investigators aim to not only reduce existing shoulder pain, but also to prevent the onset of new pain.

The current study will teach the same 4 simple shoulder strengthening exercises performed in the prior study to patients with healthy shoulders. Half of the patients will receive 2 sessions of one-to-one training with a physical therapist, and the other half will receive 4 sessions of training combined with an interactive education program on techniques to protect their shoulder in a class format led by a physical therapist and a peer mentor with a spinal cord injury. Patients will be followed for 3 years to learn if they develop shoulder pain.

02

Conditions studied

  • Spinal Cord Injury
  • Shoulder Pain

Keywords

  • Spinal Cord Injury
  • Shoulder Pain
  • Exercise
03

In context

Shoulder Pain

707 studies on the registry are indexed under Shoulder Pain; 152 are open to participants now.

This study's enrollment of 148 is above the median of 60 across 561 interventional studies indexed under Shoulder Pain.

Browse Shoulder Pain studies →

Lead sponsor

Rancho Research Institute, Inc. is the lead sponsor of 3 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • spinal cord injury
  • at least 2 years duration post spinal cord injury and no greater than 20 years duration post spinal cord injury
  • at least 18 years of age
  • free of shoulder pain that interferes with daily activities or requires medical intervention at the time of enrollment in the study
  • a total score on the "Wheelchair User's Shoulder Pain Index" of 10 or less
  • adequate arm strength and movement to perform the shoulder exercise program

Exclusion criteria

Exclusion Criteria:

  • positive shoulder impingement signs (positive Hawkins-Kennedy test and painful arc in shoulder abduction or flexion)
  • biceps tendonitis (positive Speed's test)
  • adhesive capsulitis, or cervical radiculopathy
  • a history of shoulder injury or surgery or orthopedic or neurologic disorders (other than SCI) that would impact arm function
05

Study design

Phase
Not applicable
Primary purpose
Prevention
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
148 participants (actual)

Study arms

  • Experimental
    One-to-one training group for shoulder home exercise program

    Patients will attend two sessions of one-to-one training with a physical therapist to learn the shoulder home exercise program. The sessions are 4 weeks apart. They will also review a handout on techniques to protect their shoulder during wheelchair propulsion and transfers.

    Other: Shoulder home exercise program

  • Active comparator
    Enhanced training group for shoulder home exercise program

    Patients will attend four classes held each week for 4 consecutive weeks. The classes are led by a physical therapist and a peer mentor (with a spinal cord injury). Two to four research patients are in each class. Classes begin with an interactive education presentation on techniques and recommendations to protect the shoulder during transfers, wheelchair propulsion, raises and activities of daily living. This is followed by performance of the home exercise program. Patients will be called every 3 to 6 months by a peer mentor to receive encouragement, praise, and/or problem solve barriers to exercise.

    Other: Shoulder home exercise program

  • No intervention
    Historical control group

    Historical control group has received no intervention. Eligibility criteria, outcome measures and study duration for historical control group is matched for the experimental group and active comparator.

Interventions

  • OtherShoulder home exercise program

    Patients receive instruction and practice on the shoulder home exercise program, receive a notebook with handouts including pictures and written instructions on how to perform the program, and receive a kit containing the exercise equipment. Patients are asked to perform the exercises at home 3 days a week over the next 3 years.

06

What researchers measure

Primary outcomes

  1. Presence of shoulder pain

    Presence of shoulder pain will be measured using the "Wheelchair User's Shoulder Pain Index". This questionnaire uses a visual analog scale to rate level of shoulder pain during the previous week while performing 15 common daily activities such as transferring from the bed to a wheelchair or pushing a wheelchair \> 10 minutes.

    Time frame: 36 month (3 year) evaluation time point

Secondary outcomes

  1. Activity levels

    Patients will be called every 2-3 months to report the frequency and intensity of their shoulder exercise program. Patients will be asked questions about their arm use specific to their functional abilities during the previous 1 to 3 days, such as the number of transfers performed, number of depression raises performed, how often they use their arms for chores or use their arms to help with walking (if applicable). All patients with a manual wheelchair will have an odometer installed on their wheelchair and will report their distance and speed of wheelchair propulsion.

    Time frame: Baseline and every 2-3 months over the 3 year study

Other outcomes

  1. Shoulder torque

    Shoulder torque testing will be performed using either a Biodex machine or a handheld dynamometer for the motions of isometric shoulder abduction, adduction, flexion, extension, internal rotation and external rotation.

    Time frame: Baseline, 18 month, and 36 month evaluation time points

  2. Self-Efficacy

    Patients will complete a questionnaire rating their confidence or self-efficacy in regards to exercise.

    Time frame: Baseline, 18 month and 36 month evaluation time points

  3. Community Participation

    Patients will asked to complete the questionnaire, "Reintegration To Normal Living Index".

    Time frame: Baseline, 18 month and 36 month evaluation time points

07

Study locations

1 site
  • Rancho Los Amigos National Rehabilitaiton Center
    Downey, California 90242, United States
08

References and documents

Publications

  • Mulroy SJ, Thompson L, Kemp B, Hatchett PP, Newsam CJ, Lupold DG, Haubert LL, Eberly V, Ge TT, Azen SP, Winstein CJ, Gordon J; Physical Therapy Clinical Research Network (PTClinResNet). Strengthening and optimal movements for painful shoulders (STOMPS) in chronic spinal cord injury: a randomized controlled trial. Phys Ther. 2011 Mar;91(3):305-24. doi: 10.2522/ptj.20100182. Epub 2011 Feb 3. PubMed 21292803 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 11, 2018, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT02135978
Lead sponsor
Rancho Research Institute, Inc.
Collaborators
Rancho Los Amigos National Rehabilitation Center
Responsible party
Sara Mulroy (PhD, PT, Director Pathokinesiology Service, Rancho Research Institute, Inc.) — Principal investigator
First posted
May 12, 2014
Start date
Apr 2012
Primary completion
Jul 2017
Completion
Jul 2017
Last update
Apr 11, 2018

Study contacts

Sara J Mulroy, PhD, PT
principal investigator · Rancho Research Institute and Rancho Los Amigos National Rehabilitation Center

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Apr 2018. You cannot join it, but the record below documents what was studied.

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