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Training Non-Anesthesia Personnel to Perform Nerve Blocks in Microgravity (Block-aid)

25 settembre 2026 aggiornato da: Jon Bailey, Nova Scotia Health Authority

Training Non-Anesthesia Personnel to Perform Nerve Blocks in Microgravity: A Prospective Cohort Study

Space exploration is rapidly progressing with multiple upcoming missions planned to the moon and International Space Station, and projected missions to Mars in the early 2030s. Multiple types of injuries and surgical emergencies are possible during space travel. With the rapidly increasing number of travelers, healthcare providers need to refine our plans for responding to surgical emergencies in space.

It may not be possible to return injured crew members to earth for medical treatment depending on distance from earth and the severity of the injury. Furthermore, the casualty's physiologic changes in microgravity, and logistical limitations of repatriation make addressing medical emergencies challenging. Pain medications and general anesthesia have side effects that can impact safety in space and have worse side effect profiles when compared to on earth.

Regional anesthesia, injecting local anesthetic near to a nerve(s) to create a large area of numbness on the body, has been used for many years for pain management and to allow for surgery in remote settings on earth. Military personnel have used these techniques to provide effective pain control for evacuating wounded soldiers, while maintaining their cognition. For these reasons, regional anesthesia (aka 'nerve block') has been promoted as a viable solution for injured astronauts.

Our team has demonstrated that simple nerve blocks are possible in simulated microgravity among trained anesthesia providers. Recognizing that non-physician medical technicians may be integral to future space missions, this study aims to ascertain the feasibility of training such personnel to perform simple nerve blocks in microgravity.

Panoramica dello studio

Stato

Completato

Condizioni

Intervento / Trattamento

Descrizione dettagliata

With the burgeoning human presence in space, the need to prepare for medical emergencies in microgravity environments becomes increasingly critical. Space is an inherently hazardous environment, with 21 known fatalities. Most injuries occur during lift off or re-entry, but in-flight incidents have also been reported, including fires, blunt injuries, vehicular collisions, and loss of environmental controls. Extraction times vary significantly, with the potential for hours in low-earth orbit (LEO), days from the Moon, and months from Mars. In this case or during more distant space exploration, damage control procedures may be necessary.

If astronauts are injured, physiologic and logistic complexities necessitate a different approach from hospital-based care on Earth. In addition, due to ergonomic challenges of microgravity. Systemic pain medication is not optimal in that it can cause sedation, confusion, and even delirium. This could compromise safety for the crew given the small numbers of personnel who play critical roles. If a surgical intervention was required, general anesthesia is problematic for multiple reasons.

The benefits of regional anesthesia (nerve blocks) have been recognized in remote settings, including regions with fewer resources and trained providers. Regional anesthesia limits airway management, ventilation, and hemodynamic changes. The equipment is portable, offers stable hemodynamics, effective analgesia, minimal need for supplemental oxygen, and improved alertness. As each crew member's role is pivotal for mission success, regional anesthesia ensures their cognitive participation. Our group has shown that nerve blocks are feasible in a simulated microgravity environment when performed by anesthesiologists and anesthesia residents.

In specialized teams such as astronauts, rigorously trained for space exploration, there might not be the depth of personnel to allow physicians on crews. At the current time, most missions have a single Crew Medical Officer (CMO) who is usually not a physician. Space travel with its associated communication and logistical delays further emphasizes the need for such medical training so they can act without real-time guidance.

Aim Recognizing that non-physician medical technicians may be integral to future space missions, our study aims to ascertain the feasibility of training such personnel to perform simple nerve blocks in microgravity.

Hypothesis The investigators hypothesize that despite training about nerve block mechanics and ultrasound imaging, non-physician personnel have worse accuracy, time to injection, and ease of needle placement in a simulated microgravity environment than compared to normal gravity conditions. Furthermore, the investigators hypothesize that accuracy, time to injection, and ease of needle placement will be inferior to anesthesia providers in a simulated microgravity environment.

Methods This will be a prospective cohort study using within- and between-subjects comparisons. This study will assess the ease and success of ultrasound-guided injections ("nerve blocks") by non-anesthesia personnel comparing normal gravity to microgravity conditions using a meat model. Secondly, the ease and success rate of non-anesthesia participants will be compared to anesthesia participants.

Recruitment and Allocation The investigators will recruit 20 non-anesthesia military personnel and 5 anesthesia providers who are trained scuba divers. Inclusion criteria for the non-anesthesia group would be adult (age >18 years) certified scuba divers and those who have not had prior nerve block technique training. Inclusion criteria for the anesthesia group are that they are staff anesthesiologists or senior residents and certified scuba divers since nerve block training is part of basic anesthesia training.

Training session Recruited participants would be given a 4-hour training session on ultrasound imaging theory and practical optimization, needle visualization and control, basics of local anesthetics, basic sono-anatomy, and complications of nerve blocks. This session will be developed and led by regional anesthesia fellowship trained team members. There will be opportunities to practice image acquisition and needle placement with feedback. This session will take place the day before the study.

Meat model creation All injections will use a meat model. This meat model using beef muscle, beef tendon, and ballistics gel has been previously validated for accessing accuracy of US-guided injections.

Gravity conditions In the normal gravity condition, participants will be in a seated position with the meat model positioned in the chest wall of a mannikin, supported on a table. The ultrasound, phone, and dive case will be the same as in the microgravity condition. Participants will use hand signals to communicate with their block assistant since verbal communication will not be possible underwater.

In the microgravity condition, the participants will be scuba diving in a pool. The mannikin will be secured to a table at the bottom of the pool and they will empty their buoyancy control device (causing them to sink), effectively removing the added complexity of buoyancy control. An investigator will assist each participant with the block by positioning the meat model in the mannikin, passing equipment, and injecting the dye through a syringe once they are signalled to do so. However, the investigator will not give the participant guidance on the accuracy of the needle position or the quality of their ultrasound image.

Statistical analysis and power calculation Demographics will be collected (age, gender, prior medical training, experience with nerve blocks) and reported in aggregate for the purposes of external validity and generalizability. Outcomes will be compared between normal gravity and microgravity for non-anesthesia participants (within subjects, paired data). Outcomes will also be compared between anesthesia and non-anesthesia participants (between subjects, independent data).

Data will be analyzed using generalized estimating equations to adjust for the clustered nature of the data (i.e., blocks nested within participants). For binary outcomes (success vs. failure), a binomial outcome with a logit link will be used. For numerical outcomes, a normal distribution will be assumed, though loglinear models for skewed distributions will also be explored if they fit the data better.

Power analyses adjust sample sizes for the clustered design using the design effect method described by Bland (2004). Moreover, the design assumes 14 blocks per participant. The first a-priori power analysis is for comparing normal gravity and microgravity for non-anesthesia participants with the outcome of success vs. failure. Assuming a one-tailed alpha of 0.05, power of 80%, a normal gravity success rate of 90% and a microgravity success rate of 70%, and an intraclass correlation of 0.10, a total of 19 non-anesthesia participants will be required.

The second a-priori power analysis is for comparing normal gravity and microgravity for non-anesthesia participants for time to block, which has been used as a measure of ease in learning curve studies. Assuming a one-tailed alpha of 0.05, power of 80%, a mean difference of 12 seconds, a standard deviation of 23 seconds (based on data from our prior study), and an intraclass correlation of 0.10, a total of 15 participants will be needed.

Tipo di studio

Interventistico

Iscrizione (Effettivo)

30

Fase

  • Non applicabile

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Luoghi di studio

    • Nova Scotia
      • Dartmouth, Nova Scotia, Canada, B2Y 4K9
        • Survival Systems Training Limited

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

18 anni e precedenti (Adulto, Adulto più anziano)

Accetta volontari sani

No

Sessi ammissibili allo studio

Tutto

Descrizione

Inclusion Criteria for the non-anesthesia group:

  • adult (age >18 years)
  • certified scuba divers
  • no prior nerve block technique training.

Inclusion criteria for the anesthesia group:

  • staff anesthesiologists or senior residents
  • certified scuba divers

Exclusion Criteria:

  • active ear nose and throat conditions that prevent ear equalization
  • neuromotor conditions interfering with fine motor skills
  • pregnancy
  • inability to consent

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Scienza basilare
  • Assegnazione: Randomizzato
  • Modello interventistico: Assegnazione incrociata
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Simulated Microgravity

In the microgravity condition, the participants will be scuba diving in a pool. The mannikin will be secured to a table at the bottom of the pool and they will empty their buoyancy control device (causing them to sink), effectively removing the added complexity of buoyancy control. An investigator will assist each participant with the block by positioning the meat model in the mannikin, passing equipment, and injecting the dye through a syringe once they are signaled to do so. However, the investigator will not give the participant guidance on the accuracy of the needle position or the quality of their ultrasound image.

Neutral buoyancy underwater

Comparatore attivo: Normal gravity

In the normal gravity condition, participants will be in a seated position with the meat model positioned in the chest wall of a mannikin, supported on a table. Participants will use a high-frequency (4-13 MHz) linear transducer and a 22G 50 mm echogenic needle to inject the meat model with 1-2 ml of water mixed with blue food coloring. The ultrasound, phone, and dive case will be the same as in the microgravity condition. Participants will use hand signals to communicate with their block assistant since verbal communication will not be possible underwater.

Same procedure on land

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Injection success
Lasso di tempo: 3.5 minutes

Post-injection the models will be stored in a refrigerator for at least 24 hours to dry and allow the dye to settle. Two blinded investigators will dissect the models and score them. A successful nerve block will be defined as visible blue dye staining the outside of the beef tendon without evidence of injection inside of the tendon. The presence of primarily intraneural or intramuscular staining will be considered a failed block.

3.5 minutes

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Time to injection
Lasso di tempo: 3.5 minutes

Defined as the time from the transducer first touching the nerve block model to when the needle was removed from the model.

Time was censored at 3.5 minutes, such as the participants were signalled to stop at the maximum time and the attempt was recorded as incomplete (due to time constraints).

3.5 minutes
Number of needle passes
Lasso di tempo: 3.5 minutes

Any needle passes that appeared to contact the tendon (simulated nerve), judged by noticeable movement of the tendon, were be recorded by the investigator. The number of needle passes were also recorded, judged as the number of times the needle was withdrawn and repositioned (adjustments in trajectory were not counted).

3.5 minutes
Ease of ultrasound image acquisition
Lasso di tempo: 5 minutes

Scored immediately after each block in both conditions using a 5-point Likert scale (1 = very difficult, 2 = difficult, 3 = neutral, 4 = easy, 5 = very easy).

5 minutes
Ease of needle placement
Lasso di tempo: 5 minutes

Scored immediately after each block in both conditions using a 5-point Likert scale (1 = very difficult, 2 = difficult, 3 = neutral, 4 = easy, 5 = very easy).

5 minutes
Intraneural injection
Lasso di tempo: 3.5 minutes

Post-injection the models were be stored in a refrigerator for at least 24 hours to dry and allow the dye to settle. Two blinded investigators dissected the models to score the position of the dye. The presence of dye within the tendon will be considered an "intraneural" injection.

3.5 minutes

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Sponsor

Pubblicazioni e link utili

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Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Effettivo)

20 marzo 2026

Completamento primario (Effettivo)

29 marzo 2026

Completamento dello studio (Effettivo)

29 marzo 2026

Date di iscrizione allo studio

Primo inviato

17 settembre 2026

Primo inviato che soddisfa i criteri di controllo qualità

25 settembre 2026

Primo Inserito (Effettivo)

30 settembre 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

30 settembre 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

25 settembre 2026

Ultimo verificato

1 settembre 2026

Maggiori informazioni

Termini relativi a questo studio

Altri numeri di identificazione dello studio

  • REB # 2024-7417

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

INDECISO

Descrizione del piano IPD

Ability to share would be based on ethical and Canadian Armed Forces approval on a case by case basis.

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .