Long-term Medical Impact of War Injuries on Military Personnel

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorDirection Centrale du Service de Santé des Armées

About this trial

Beyond short-term multidisciplinary care, the French Armed Forces Health Service provides medical and surgical care, followed by medical and social care and long-term support for the wounded, especially when they have suffered multiple injuries during operations and are severely disabled. This involves primary phases of rehabilitation to limit the after-effects, preserve the functional prognosis and increase the autonomy of the injured person; secondary medical and social phases of rehabilitation and reintegration to restore the injured person's place in society.

The reconstruction stages are therefore essential. However, little data is available on the evolution of these patients' general health.

A similar follow-up cohort was set up by the British Army to monitor physical injuries during the conflict in Afghanistan. The results suggest the possibility of long-term cardiovascular and neoplastic complications in this population.

Furthermore, there is no data available on the evolution of the health status of war wounded in France. A retrospective study is currently underway, TRAUM-IMPACT RETRO, with the aim of assessing the consequences of 10 years of operational engagements from 2013 to 2023. This study should enable the medical French army service to clarify the topography of injuries and the medical and social outcomes of casualties treated at the Percy National Military Institute of Surgery (HNIA Percy) during this period. Initially, a pilot study followed by a cohort study will enable the investigators to standardise the medical follow-up of war casualties and determine their medical and social outcomes.

The population studied in this clinical trial corresponds to all military personnel repatriated and treated at the Percy National Military Hospital for a war injury defined as follows: "Any physical injury of a certain degree of severity directly related to the presence of the enemy, i.e. in combat or indirectly through effective participation in war operations, preparatory to or consequential to combat. " The investigators hypothesise that severely disabled wounded soldiers are at risk of specific complications leading to excess morbidity and disability, complications associated with ageing, and a risk of social and professional isolation. As a result, the participants require lifelong monitoring to prevent, detect and manage these complications, thereby ensuring that the nation gives its wounded children the recognition the participants deserve.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age ≥ 18 years

French military patient

Patient wounded in action

Patient repatriated and treated at the Percy National Military Hospital for a physical war injury sustained between 2020 and 2025

Disqualifiers

Isolated psychological injury

Physical injury not related to war

Patient unable to give free consent, under guardianship or curatorship

Refusal to participate

Trial design

Design model

Single group

Treatments tested in this trial

  • biological and radiological examinations

    Other intervention

    The TRAUM-IMPACT study designed to assess the feasibility of establishing a long-term cohort study to monitor war casualties and will be carried out in parallel with the usual care provided.

Treatment groups

20 Participants
are divided into 1 treatment group
Group A: War wounded repatriated and treated at the Percy National Institute of Military MedicineExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

The primary outcome is the feasibility of a standardized multidisciplinary follow-up strategy, assessed by patient recruitment rate, retention rate during follow-up, completion

Health event reported during visits over the course of the study and type of injury at inclusion (multiple trauma, limb trauma, head trauma).

Time frame
2 years

Secondary outcomes

1

Longitudinal evolution of quality of life according to type of injury

Short-Forme (SF) 36 quality of life score

Time frame
2 years
2

Longitudinal changes in gait performance

Gait performance will be evaluated using both clinical and instrumented assessments, including walking speed, walking perimeter, Timed Up and Go (TUG) test, wearable sensor-based gait analysis (spatiotemporal gait parameters), static postural assessment, and balance evaluation. These measures will be used to quantify changes in mobility, stability, and functional recovery throughout follow-up.

Time frame
2 yaers
3

Define predictive factors for the occurrence of a new diagnosis or new treatment (psychiatric illness, chronic illness, cardiovascular disease, neoplasia, or any relevant medical event).

Search for the occurrence of a new diagnosis or new treatment (psychiatric illness, chronic illness, cardiovascular disease, neoplasia, or any relevant medical event) and predictive factors.

Time frame
2 yaers
4

Level of generic pain

Generic pain questionnaire (QDSA)

Time frame
2 years

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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