Managing the Ick Factor for Space Readiness
IAC · Space Human FactorsWTSA Space Sensory Lab

Managing the Ick Factor for Space Readiness

Historic approaches & future opportunities for nausea, menstruation, and excrement — three expressions of one perceptual-containment problem across the LEO-to-lunar arc.

Thesis

Nausea, menstruation, and waste are one perceptual-containment system with three expressions, and the binding constraint on each migrates as missions move outward, from acute containment in LEO to chronic, loop-compatible, whole-body risk on the Moon.

The ick continuum · three domains

yum ⟷ ick · a single perceptual axis governing intake, morale, endurance
01 / NAUSEA

Nausea

space adaptation syndrome · emesis containment

60–90% of crew, first ~72 h of orbital flight. In microgravity it is floating droplets, not odor, that propagate nausea — "in orbit you couldn't smell it" (Sacco, interview). Seventy years, no consensus countermeasure.

Forward provocation below
02 / MENSTRUATION

Menstruation

suppression · containment · hidden physiological cost

Managed largely by hormonal suppression — because the containment and hygiene burden is intolerable. That choice carries a circulatory and skeletal cost no one has measured against the mission.

Flagship · live below
03 / EXCREMENT

Excrement

MAG extended-wear · containment · skin integrity

"Am I clean, and will nothing float out when I leave the seat?" (Sacco). Extended-wear maps onto terrestrial incontinence-associated dermatitis; hydration-restriction to avoid voiding maps onto "nurse's bladder."

Forward provocation below
containment intolerability drives the clinical risk  ·  the ick is not downstream of the science — it is upstream of it
Menstrual suppression stacks two prothrombotic exposures nobody has studied together

Suppression is chosen because containment in microgravity is intolerable — the water-recovery loop cannot process menstrual blood, and privacy and hygiene are scarce. But suppression is not free. Spaceflight and hormonal suppression each raise thrombotic risk through different mechanisms, and the mission environment simultaneously attacks bone — the same axis one common method depletes.

Exposure A · the environment

Venous stasis from headward fluid shift

An 11-crew ISS ultrasound study found stagnant and retrograde jugular flow, with confirmed internal jugular vein thrombosis in at least one astronaut — a newly identified spaceflight risk. The index case had no VTE history; unprovoked IJV thrombosis is uncommon on Earth. Parabolic data show the venous change is graded by gravity level.

Marshall-Goebel et al. 2019, JAMA Netw Open · NEJM 2019 case
Exposure B · the countermeasure

Estrogen & the suppression method itself

Combined hormonal contraceptives — the default suppression route — raise venous thromboembolism risk ~2–4× and ischemic-stroke risk ~1.6×, graded by estrogen dose. Depot progestin (DMPA) carries an FDA black-box warning for bone-density loss. The levonorgestrel IUD is the one hormonal method not linked to elevated clot risk.

Cochrane / meta-analyses 2014–2018 · US FDA DMPA label
Method × risk — binding constraint at low earth orbit
Suppression methodThrombosis axisBone axis
Combined pillestrogen + progestin VTE 2–4× · stroke ~1.6×
compounds spaceflight venous stasis
neutral
no established bone effect
DMPA depotprogestin injectable differing profile
progestin-only; data mixed
BMD · black-box warning
compounds skeletal unloading
LNG-IUDlevonorgestrel, local no elevated risk
the terrestrial off-ramp
minimal systemic effect
local delivery
LEO · short-duration: interaction largely academic — Shuttle-era crews often time-shifted cycles rather than suppressing (Baker, oral communication). No method is binding over days.
Where the standard is silent

NASA holds the jugular-thrombosis finding and the spaceflight bone-loss evidence separately. Neither is linked to menstrual-suppression method selection in current guidance. The interaction is uncharacterized.

Open question

Does long-duration spaceflight plus estrogen-containing suppression produce additive thrombotic risk — and does estrogen-suppressing depot compound spaceflight bone loss? Each exposure is established; their interaction in a menstruating crewmember has never been measured.

Looking forward · design stance

Design for adaptation, not just containment

The body adapts — Sacco and Baker both testify to it. But adaptation has a cost the current architecture ignores: the loss of normalcy, and the psychological load of managing your own body in a confined space with no privacy. The forward move is to shift the intervention from the moment of failure to the whole person, across the whole mission — profiled before flight, monitored through it, supported culturally and psychologically within it.

Tier: design stance + open provocation · not validated result
01

Preflight profiling & personalization

No two humans respond alike — SAS susceptibility, suppression trade-off, and skin/continence response are all person-specific. Calibrate the individual, not the average crew.

anchor: "individualized approach is key" (Nelson); "a suite of options" (Baker)
02

In-flight biometric recalibration

Continuous physiological monitoring across gravity transitions to detect adaptation changes — replacing episodic self-report, which stigma makes unreliable. Requirement: monitoring that survives real compliance.

caveat: "give me a watch, it's on the shelf by day 2" (Nelson)
03

New rituals & evolving culture

Adaptation is cultural too. Rituals for managing the body without shame, and a reporting culture where symptoms aren't penalized — because what isn't reported can't be designed for.

"astronauts aren't forthcoming — it affects certification" (Baker)
04

Psychological normalcy & longevity

The human adapts but will miss normalcy. Designing for that missing — focus, relaxation, performance, long-term health — is itself the innovation, not an afterthought to containment.

the wellbeing target: mental focus · efficiency · endurance
ground transit surface  ·  one continuous person, not a sequence of failures to contain
Forward provocations · one per domain, mission-matched Level 2 — direction & requirement, not mechanism · each keyed to a NASA gap + terrestrial analog
01 · Nausea / SAS

From symptom suppression to predictive pre-conditioning

Countermeasures were optimized against the symptom, not the mission day — a drug that sedates, by a route that hurts, on a schedule set by crew sleep. The requirement: accelerate the adaptation the body will make anyway, and manage symptoms without a cognitive tax.
SHORT LEOease the single microgravity-entry transition; non-sedating countermeasures for the first 72 h.
LUNARrepeated transitions + degraded surface reference frame + the uncharacterized 0.16 g dimension (only 14 humans, ever).
NASA gap: SAS guidance ISS-baselined; partial-g unaddressed · analog: vestibular rehab & cybersickness medicine
02 · Menstruation

Loop-compatible management + a personalized suppression decision

The requirement is not better absorbency — it is material & waste-stream compatibility with a closing recovery loop, plus a decision framework that weighs the thrombosis-vs-bone trade-off against mission profile rather than defaulting to one method.
SHORT LEOconsumables tolerable; containment & hygiene dominate.
LUNARreuse & loop-compatibility bind; suppression runs months–years, activating the two-exposure interaction above.
NASA gap: recovery loop can't ingest blood; thrombosis + bone data unlinked to method · analog: contraception pharmacovigilance
03 · Excrement / MAGs

From disposable container to sensed, loop-compatible interface

Reframe the garment as an interface, not a bag: microclimate & skin-integrity sensing to close the "am I clean / is my skin breaking down" gap, with a material end-of-life matched to the mission's recovery architecture.
SHORT LEOcompaction / water-recovery pathway; skin-integrity over hours of suited wear.
LUNARpyrolysis / plant-media pathways; extended campaigns make reuse and skin health binding.
NASA gap: [V2 11013] sets containment, no skin-microclimate or loop requirement · analog: incontinence-associated dermatitis science
Signature artifact · design provocation

The emesis bag, reimagined as an active interface

"We used to have an emesis bag — we called it the microgravity carnation. We kept it in our left front pocket so we could get at it very quickly." — Sacco, interview

An emesis interface that couples reliable microgravity sealing with controlled aromatic release — pre-emptively, and for psychological recovery afterward. Framed at the requirement level: the calming-terpenoid class is named, the specific agent left open. The material is loop-compatible / mission-architecture-matched, not merely "biodegradable" — there is nothing to biodegrade into in a closed cabin.

Gingerantiemetic half
gut-acting, non-sedating

Reduces nausea severity and rescue-antiemetic use across meta-analyses; effect on vomiting is mixed. Acts on the gut, not centrally — so it avoids the cognitive cost that defines the flight formulary's problem.

peer-reviewed · contested magnitude
Calming terpenoid aromaticsrelaxation +
post-emesis recovery

A compound class — linalool, citral, geraniol-bearing botanicals (lavender, lemongrass, relatives) — anxiolytic in animal models via GABAergic / serotonergic modulation. Class named, specific agent open. Two unknowns stack: the pathway is contested, and microgravity attenuates the olfaction these compounds may depend on.

open question · mechanism & in-flight route unresolved
The gap is the point: every candidate aromatic/nutritional countermeasure has an evidence gap that is specifically worse in the attenuated-olfaction microgravity environment. Resolving it requires chemosensory-in-partial-gravity work.
Evidentiary tiering: peer-reviewed astronaut oral communication open research question
Marshall-Goebel K, et al. Assessment of jugular venous blood flow stasis and thrombosis during spaceflight. JAMA Netw Open. 2019;2(11):e1915011. Auñón-Chancellor SM, et al. Venous thrombosis during spaceflight. N Engl J Med. 2020;382:89–90. Roach REJ, et al. Combined oral contraceptives: risk of myocardial infarction and ischemic stroke. Cochrane Database Syst Rev. 2015. Oedingen C, et al. Systematic review & meta-analysis of COC and VTE risk. Thromb Res. 2018. US FDA. Depo-Provera (DMPA) boxed warning: bone mineral density loss. Jain V, Wotring VE. Medically induced amenorrhea in female astronauts. npj Microgravity. 2016;2:16008. Baker ES. Oral communication, interview, 2025 (with consent). Harada H, et al. Linalool odor-induced anxiolytic effects in mice. Front Behav Neurosci. 2018;12:241. Costa CARA, et al. Anxiolytic-like effect of Cymbopogon citratus (lemongrass) essential oil; GABAergic mechanism. Agatonovic-Kustrin S, et al. Anxiolytic terpenoids & aromatherapy: linalool, geraniol, citral — GABA/glutamate modulation. Tóth B, et al. / Chang & Ismail. Ginger for postoperative nausea: meta-analyses, 2006–2021 (contested). Marshall-Goebel K, et al. Jugular flow & partial gravity; verticality threshold 0.16–0.38 g (parabolic). Beheshti-Rooy / Gray M, et al. Incontinence-associated dermatitis & moisture-associated skin damage. Nerbass FB, et al. Fluid restriction, delayed voiding & UTI in nurses ("nurse's bladder").