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Efficacy of a Criteria Based Clinical Pathway for Rehabilitation of Shoulder Injuries

Efficacy of a Criteria Based Clinical Pathway for Rehabilitation of Shoulder Injuries

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06536114
Acronym
CRISP
Enrollment
250
Registered
2024-08-02
Start date
2025-03-01
Completion date
2027-08-30
Last updated
2024-08-02

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

Conditions

Shoulder Injuries, Shoulder Pain

Keywords

shoulder, return-to-duty, physical therapy, rehabilitation

Brief summary

The goal of this clinical trial is to compare the current standard of care for rehabilitation of non-operative shoulder injuries to a novel, criteria-based approach (CRISP). Additionally, this study will identify factors which contribute to return to duty readiness. The main questions it aims to answer are: * Are there differences in patient reported outcomes between participants who undergo the criteria-based rehabilitation program versus the standard of care for shoulder injuries? * Are there differences in clinical measures (strength, etc.) between participants who undergo the criteria-based rehabilitation program versus the standard of care for shoulder injuries? * Are there clinical or rehabilitation factors, or participant characteristics, that contribute to return to duty readiness? Participants will be randomized to either complete their rehabilitation per the standard of care with a physical therapist in a Military Treatment Facility or complete the CRISP program with a research physical therapist. Participants will: * Attend physical therapy for a non-operative shoulder injury * Attend initial and final clinical assessments at the clinic * Complete patient reported outcomes at 1-, 3-, 6- and 12-month timepoints

Detailed description

Without a data-driven pathway to assess and rehabilitate shoulder injuries, clinicians may be using time rather than criteria to guide rehabilitation and clearance for return to duty. Delayed return to duty and subsequent injury or surgery contribute to time lost from duty, negative financial implications for the Military Health System, and adversely affect Service members' mental health and quality of life. Therefore, we propose a study determining the optimal treatment progression to reduce unnecessary variability in management of non-operative of shoulder injuries for Service members through a phased, criteria-based clinical pathway: Criteria-based Rehabilitation for Injured Shoulders Paradigm (CRISP). Additionally, this study will identify factors which contribute to return to duty readiness. To demonstrate the benefits of the CRISP program, we will determine the differences in physical, psychological, and quality of life patient-reported questionnaires, and clinical assessments of shoulder strength and function between the novel criteria-based rehabilitation program and the current standard of care for Service members with non-operative shoulder injuries within the Military Health System. To accomplish this, we will conduct a multi-site, single-blinded, randomized controlled trial in active duty Service members seeking care for a non-operative shoulder injury referred to physical therapy. We will recruit 250 Service members from the Naval Medical Forces (Pacific Region) and Brooke Army Medical Center/Center for the Intrepid. Participating Service members will complete clinical assessments and questionnaires at initial and final assessments; additionally, a link will be sent to participants to fill out questionnaires virtually at 1-, 3-, 6-, and 12-month time intervals. The CRISP group will undergo physical therapy treatment, directed by a research physical therapist, including both supervised physical therapy and a guided home exercise program. This approach has three phases: stabilization, for joint protection; strength and endurance, for functional capacity; and power, to prepare the Service member for returning to previous level of duty. The standard of care group will serve as the control arm and complete a period of physical rehabilitation under the supervision of a Military Health System physical therapist without study-specific guidance or interventions. To our knowledge, this is the first study to compare a criteria-based exercise intervention approach to the usual standard of care for the conservative treatment of shoulder injuries as well as identifying factors which contribute to RTD readiness. Without using a data-driven pathway to assess and rehabilitate shoulder injuries, Service members may experience a potential delay in returning to their previous military occupational specialty or deployability, and residual impairments may persist. In turn, this could lead to a higher incidence of re-injury or referral to surgical intervention. In the near-term, the findings from this study will enhance individual patient care within the MHS, accelerating return to duty for our Service members and with fewer physical limitations. We also anticipate our findings will help identify the predictors of shoulder function and return to duty readiness. This study's findings will directly influence patient care by elucidating which treatment paradigm optimizes shoulder function in Service members, ultimately leading to improvements in quality of life for Service members, reducing time lost from injuries, as well as maximizing Service members' readiness, unit cohesion, and mission accomplishment.

Interventions

OTHERCRISP: Criteria-Based Approach for the Rehabilitation for Non-Operative Shoulder Injuries

The CRISP group will undergo physical therapy treatment, directed by a research physical therapist, including both supervised physical therapy and a guided home exercise program. This approach has three phases: stabilization, to facilitate joint protection; strength and endurance, to optimize functional capacity; and power, to prepare the Service member for returning to previous level of duty.

OTHERStandard of Care

The Standard of Care group will serve as the control arm and complete a period of physical rehabilitation under the supervision of a Military Health System physical therapist without study-specific guidance or interventions.

Sponsors

Brooke Army Medical Center
CollaboratorFED
Congressionally Directed Medical Research Programs
CollaboratorFED
Henry M. Jackson Foundation for the Advancement of Military Medicine
CollaboratorOTHER
The Geneva Foundation
CollaboratorOTHER
United States Naval Medical Center, San Diego
Lead SponsorFED

Study design

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

Masking description

The outcomes assessor will not be a physical therapist and thus not involved with the participant's medical treatment.

Intervention model description

multi-site, single-blinded, randomized controlled trial

Eligibility

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

Inclusion criteria

* Active-duty Service members over the age of 18 who are seeking medical attention for shoulder pain or injury will be recruited to participate in this study.

Exclusion criteria

* The

Design outcomes

Primary

MeasureTime frameDescription
Penn Shoulder ScoreInitial and final clinical study assessments; 1-, 3-, 6- and 12-months post-randomizationPatient-reported outcome with shoulder pain, satisfaction, and function subscales

Secondary

MeasureTime frameDescription
Referral to Surgical Intervention3-, 6-, 12- monthsParticipant was referred to surgical invention for their shoulder injury.
Patient-Reported Outcomes Measurement Information System (PROMIS®)Initial and final clinical study assessments; 1-, 3-, 6- and 12-months post-randomizationPatient-reported outcome measuring physical, mental, and social health among individuals with various chronic conditions.
Optimal Screening for Prediction of Referral and Outcome- Yellow Flag (OSPRO-YF)Initial and final clinical study assessments; 1-, 3-, 6- and 12-months post-randomizationThe OSPRO-YF is a 10-item screening tool which incorporates several psychosocial domains, namely, mood, fear avoidance, and positive affect-coping.
Military Orthopaedics Tracking Injuries and Outcomes Network (MOTION) Readiness Rehab QuestionnaireInitial and final clinical study assessments; 1-, 3-, 6- and 12-months post-randomizationThe Readiness Rehab Questionnaire assesses deployment readiness, containing questions including, if called for a 6 month deployment today, my confidence to travel to/within a combat zone, carry/wear/use all required equipment and/or weapon, and perform required military duties for the duration of the 6 month deployment is: and my confidence to do my specific military duties with well managed pain is:\_\_, both scored on 0-100 scales.

Countries

United States

Contacts

Primary ContactMarisunta Pontillo, PhD
marisunta.l.pontillo.civ@health.mil215-266-1904
Backup ContactSara Gorczynski
sara.r.gorczynski.ctr@health.mil619-532-9704

Outcome results

None listed

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