Actively Recruiting

Age: 18Years +
All Genders
NCT07031791

PETRA: Pictorial Assessment of Task Occurrence and Upper Limb Avoidance Behaviors

Led by University Hospital, Angers · Updated on 2025-12-29

200

Participants Needed

1

Research Sites

104 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The clinical evaluation of patients suspected of having thoracic brachial outlet syndrome (TBS) is not standardized, as it may be for the lower limbs. Assessment of symptoms and functional impact is based on questionnaires (Disability of the Arm, Shoulder and Hand: DASH, Short Form 36: SF36, Mobility of the Arm and Shoulder: MASC, Thoracic and Upper limb ischemia Pain: TULIP), which are complex to complete, sometimes non-lateralized, and do not take into account the frequency of occurrence of certain gestures or the avoidance behaviours adopted by patients. For avoidance behaviors, a recent tool has been proposed in the form of the Avoidance Daily Activities Photo Scale (ADAP shoulder scale). However, this questionnaire has not been translated into French and does not reflect the frequency with which patients are confronted with the different tasks proposed. The aim of this study is to test the feasibility of a new questionnaire (PETRA), derived from the ADAP-shoulder scale, which is simple for patients to complete, quick to analyze and calculable directly by the doctor, and suitable for the general population, whether for initial assessment or follow-up. The PETRA aims to assess avoidance behaviours in the face of daily tasks, but also the frequency of occurrence of these tasks in order to evaluate a disabling score that weights the avoidance index according to the degree of exposure to the proposed tasks. The investigators hypothesize that the PETRA questionnaire could eventually be used routinely.

CONDITIONS

Official Title

PETRA: Pictorial Assessment of Task Occurrence and Upper Limb Avoidance Behaviors

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult
  • Person referred for suspected TDSB
Not Eligible

You will not qualify if you...

  • Person unwilling to complete questionnaire and participate
  • Person unable to understand the objectives of the study

AI-Screening

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Trial Site Locations

Total: 1 location

1

Angers University hospital

Angers, France

Actively Recruiting

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Research Team

S

Simon LECOQ, MD

CONTACT

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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