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RecruitingNCT06752551Updated Jun 4, 2025

Apprehension-based Training Compared With Standard Physical Therapy for Military Personnel Following Anterior Shoulder Dislocation - a Randomized Clinical Trial

An interventional study of Apprehension-based training and Standard physical therapy in Anterior Shoulder Dislocation, sponsored by Alon Rabin. Recruiting at 1 site in Israel. Open to participants aged 18 Years to 39 Years. Per ClinicalTrials.gov, last updated 2025-06-04.

Sponsored by Alon Rabin · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Started Feb 2025; still recruiting 1 year 9 months later.
Phase
Not applicable
Study type
Interventional
Enrollment
85
Allocation
Randomized
Ages
18 Years to 39 Years
Sex
All
01

Study summary

The goal of this clinical trial is to determine if a new rehabilitation protocol (apprehension-based training), leads to better recovery after shoulder dislocation among military personnel.

Participants will be randomly allocated to apprehension-based training or standard physical therapy. In apprehension-based training participants will train to control their shoulder under progressively more unstable conditions. Standard physical therapy will be provided based on the clinical judgment of the treating physical therapist The primary hypothesis is that participants undergoing apprehension-based training will experience a more complete recovery of function, better shoulder-related quality of life, and incur less recurrent dislocations.

02

Conditions studied

  • Anterior Shoulder Dislocation

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Keywords

  • Randomized clinical trial
  • Anterior shoulder dislocation
  • Shoulder instability
  • Physical therapy
03

In context

Shoulder Dislocation

105 studies on the registry are indexed under Shoulder Dislocation; 22 are open to participants now.

This study's planned enrollment of 85 is above the median of 60 across 71 interventional studies indexed under Shoulder Dislocation.

Browse Shoulder Dislocation studies →

Lead sponsor

This is the only study on the registry with Alon Rabin as lead sponsor.

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

04

Who can participate

Ages eligible
18 Years to 39 Years
Sexes eligible
All
Accepts healthy volunteers
No

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Age 18-39 years
  • Shoulder dislocation (primary or recurrent) documented by a medical practitioner (physician, military medic)
  • Positive anterior apprehension test
  • Gross shoulder muscle strength 3/5 or greater

Exclusion criteria

Exclusion Criteria:

  • Previous shoulder fracture, tendon tear, or shoulder surgery
  • Voluntary shoulder dislocation
  • Functional (Stanmore polar III) shoulder instability
  • Dislocation associated with a motor vehicle accident.
  • Diagnosis of rheumatoid arthritis, cancer (current), fibromyalgia, psychiatric disease)
  • Current pregnancy
  • Inability to attend at least one physical therapy session every 2 weeks.
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Investigator, Outcomes assessor)
Enrollment
85 participants (estimated)

Study arms

  • Experimental
    Apprehension-based training

    Apprehension-based training is a 3-phase exercise intervention intended to expose patients to progressively increased shoulder apprehension-provoking conditions. Patients progress from one phase to the other upon completion of the previous level of exercise

    Behavioral: Apprehension-based training

  • Active comparator
    Standard physical therapy

    Standard physical therapy will be provided by a licensed physical therapist and may include exercises of different kinds, manual therapy, dry needling or electrophysiological modalities.

    Behavioral: Standard physical therapy

Interventions

  • BehavioralApprehension-based training

    This intervention is comprised of the 3 phases: Static phase - Isometric (static) exercises performed in progressively greater shoulder apprehension ("instability") provoking conditions Dynamic phase: Isotonic (dynamic) exercises using shoulder apprehension-provoking movement patterns at a gradually increasing pace of movement. Neurocognitive phase: Dynamic phase exercises are continued at a high pace with the addition of cognitive tasks ("distractions"). The intervention is guided by a physical therapist and includes up to 8 individual (one on one) sessions. In each session the physical therapist assesses exercise performance quality and when appropriate progresses exercise intensity and/or phase. Patients are expected to perform home exercises according to their phase of the program on a daily basis in between physical therapy sessions.

  • BehavioralStandard physical therapy

    Standard physical will be provided based on the assessment and judgment of the physical therapist. Intervention may include active exercises for increased shoulder mobility, muscle strength and neuromuscular control. Intervention may also include manual therapies such as massage, soft-tissue and joint mobilizations, dry needling, and electrophysiological modalities. No more than 8 individual sessions with a physical therapist will be provided over the course of treatment with some form of a home exercise program in between.

06

What researchers measure

Primary outcomes

  1. Return to preinjury level of function

    Patient's ability to resume their preinjury military and overall level of function will be assessed separately through a telephone interview 3 months after the end of their assigned intervention. This outcome will be rated dichotomously: "Yes" (have resumed my preinjury military/overall level of function), or "No" (have not been able to resume my preinjury military/overall level of function).

    Time frame: 3 months following the end of intervention

  2. Western Ontario Shoulder Instability Index

    The Western Ontario Shoulder Instability Index is a self-reported measure of shoulder instability related quality of life. This questionnaire includes 21 items regarding symptoms, activity limitations, quality of life and emotions. Each item is scored on a 100mm visual analogue scale resulting in a total score of 0 - 2100 which can be converted to a percentage with greater scores indicating greater disability.

    Time frame: Baseline to end of intervention (10 weeks) and 1-year follow-up (62 weeks).

  3. Recurrence

    Recurrent events of instability, either in the form of a frank dislocation or a sensation of instability (subluxation) will be assessed through a telephone interview.

    Time frame: One year following the end of the intervention

  4. Supine moving apprehension test

    Dynamic stability will be assessed with the supine moving apprehension test. This is a functional performance test in which the patient is asked to repeatedly move the shoulder into 135- and 180-degrees of abduction from a supine position while holding a dumbbell (2-3 kg). The number of repetitions over one minute comprises the score of the test.

    Time frame: Baseline to end of intervention (10 weeks)

Secondary outcomes

  1. Subjective shoulder value

    A patient reported single numeric assessment of shoulder function as a percent of a normal shoulder: "What is the overall percent value of your shoulder if a completely normal shoulder represents 100%?"

    Time frame: Baseline, end of intervention (10 weeks), and 1-year follow up (62 weeks)

  2. Tampa scale of kinesiophobia

    A self-reported 17-item fear of movement and reinjury measure. Each item is scored on a 4-point Likert scale for a total score between 17-68.

    Time frame: Baseline, end of intervention (10 weeks), and 1-year follow-up (62 weeks)

  3. Anterior apprehension test

    The sensation of apprehension will be assessed through the anterior apprehension test performed in 4 stages: 1.) shoulder abduction to 90 degrees; 2.) external rotation; 3.) horizontal abduction; 4.) Shoulder abduction beyond 90 degrees. Elicitation of apprehension (verbal, fascial expression, or muscle guarding) will be rated according to the stage at which it occurs (1-4). The test will be rated negative (5) if apprehension is not elicited at any stage.

    Time frame: Baseline to end of intervention (10 weeks)

  4. Shoulder internal/external rotator muscle strength

    Shoulder internal and external rotator muscle strength will be assessed using a hand-held dynamometer in a supine-lying position with the shoulder abducted 90 degrees, neutral rotation, and the elbow bent 90 degrees. The examiner will position a hand-held dynamometer over the distal anterior (internal rotator strength) or posterior (external rotator strength) aspect of the forearm and resist a maximal voluntary effort by the patient. two repetitions will be performed for each strength test with the highest value used for data analysis.

    Time frame: Baseline and end of intervention (10 weeks)

  5. Abdominal rollout

    From a kneeling position with the hands gripping a barbell loaded with a 5kg plate on each side, the patient will roll forward to the greatest distance possible and return to the starting position. The test will be performed in a narrow (shoulder width) and wide (2x shoulder width) hand grip. Up to 5 repetitions will be allowed to achieve maximum distance in each grip condition.

    Time frame: Baseline and end of intervention (10 weeks)

  6. Heart rate variability

    Heart rate variability (HRV) during apprehension provocative and non-apprehension provocative shoulder movements will be measured using a Polar H10 chest strap. Heart rate variability will serve a physiological marker for autonomic nervous system response to movement provoked stress in the context of anterior shoulder dislocation.

    Time frame: Baseline and end of intervention (10 weeks).

07

Study locations

1 of 1 sites recruiting
  • Israel Defense Forces Medical Corps
    Be'er Ya'akov, 7030732, Israel
    Recruiting
    • Netanel Hollander, MS, PT · Contactnetanel911@gmail.com · 972-52-9216908
    • Alon Rabin, PhD, DPT · Contactalonra@ariel.ac.il · 972-52-3581550
    • Netanel Hollander, MS, PT · Principal investigator
08

References and documents

Publications

  • Rabin A, Noyman L, Yaakobi N, Kazum E. Apprehension-Based Training: A Novel Treatment Concept for Anterior Shoulder Dislocation - A Case Report. Int J Sports Phys Ther. 2024 Jul 1;19(7):888-897. doi: 10.26603/001c.118928. eCollection 2024. PubMed 38966825 ↗
  • Rabin A, Chechik O, Olds MK, Uhl TL, Kazum E, Deutsch A, Citron E, Cohen T, Dolkart O, Bibas A, Maman E. The supine moving apprehension test-Reliability and validity among healthy individuals and patients with anterior shoulder instability. Shoulder Elbow. 2024 Feb;16(1):98-105. doi: 10.1177/17585732231170197. Epub 2023 Apr 18. PubMed 38435037 ↗

Individual participant data

Plan to share: Yes — Baseline, final and follow-up self-reported and physical performance outcome measures will be shared electronically.

Supporting information: Study protocol, Statistical analysis plan

Time frame: 1.1.2028-1.1.2029

Access criteria: Scholars, medical professionals as well as the general public may access outcomes measures data, intervention protocol and statistical analyses upon request from the principal investigator at the URL provided below.

Data sharing details ↗ · pniot.ariel.ac.il

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 4, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06752551
Lead sponsor
Alon Rabin
Collaborators
Medical Corps, Israel Defense Force
Responsible party
Alon Rabin (Principal investigator, Ariel University) — Sponsor-investigator
First posted
Dec 30, 2024
Start date
Feb 5, 2025
Primary completion
Dec 31, 2027 (estimated)
Completion
Dec 31, 2027 (estimated)
Last update
Jun 4, 2025

Study contacts

Alon Rabin, PhD, DPT
Contact
alonra@ariel.ac.il
972-52-3581550
Netanel Hollander, MS, PT
Contact
netanel911@gmail.com
972-52-9216908
Alon Rabin, PhD, DPT
study chair · Ariel University

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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