Background: Anthropogenic climate change has caused extreme temperatures worldwide, with data showing that sub-Saharan Africa is especially vulnerable to these changes. In sub-Saharan Africa, women comprise 50% of the agricultural workforce, often working throughout pregnancy despite heat exposure increasing the risk of adverse birth outcomes. In this study, we aimed to improve understanding of the pathophysiological mechanisms responsible for the adverse health outcomes resulting from environmental heat stress in pregnant subsistence farmers. We also aimed to provide data to establish whether environmental heat stress also has physiological effects on the fetus. Methods: We conducted an observational cohort study in West Kiang, The Gambia, at the field station for the Medical Research Council Unit The Gambia at London School of Hygiene & Tropical Medicine (named the MRC Keneba field station). Pregnant women who were aged 16 years or older and who were at 160 beats per min [bpm] or <115 bpm, or increase in umbilical artery resistance index) were measured at rest and during the working period. Multivariable repeated measure models (linear regression for FHR, and logistic regression for fetal strain) were used to evaluate the association of heat stress and heat strain with acute fetal strain. Findings: Between Aug 26, 2019, and March 27, 2020, 92 eligible participants were recruited to the study. Extreme heat exposure was frequent, with average exposures of WBGT of 27·2°C (SD 3·6°C) and UTCI equivalent temperature of 34·0°C (SD 3·7°C). The total effect of UTCI on fetal strain resulted in an odds ratio (OR) of 1·17 (95% CI 1·09–1·29; p24·8°C).11, 18 An updated sample size calculation that included an increased exposure level and that assumed an unexposed incidence risk of fetal strain to be 5% estimated that a sample size of 74 would be needed to detect an exposure incidence risk of 30%, with an α of 0·05 and a power of 80%. All analyses were conducted in R, version 4.1.0. Normally distributed continuous variables are presented as a mean with SD, non-parametric data as median and IQR, and categorical variables as counts. Heat stress exposure variables were analysed as continuous data. Outcome measures of fetal strain were analysed by both FHR as a continuous variable and fetal strain as a binary variable as defined in the Procedures and outcomes section. Initial data exploration assessed changes in mean temperature and heart rate from baseline to working state using Wilcoxon signed-rank tests. The correlation between multiple similar variables (eg, WBGT, UTCI, and air temperature) were evaluated using Pearson’s correlation. Univariable analysis of maternal heat strain (PSIMOD), fetal strain by FHR (continuous variable and linear regression), and fetal strain (binary variable and logistic regression) were conducted to explore risk factors. Final datasets in multivariable analyses were complete. The association between heat stress and maternal heat strain (by PSIMOD) was explored using linear and non-linear models.31 Non-linear models with natural and logarithmic splines with knots placed at the 50th and 90th centiles were evaluated, in keeping with other studies on the association between temperature and health outcomes. The linear model had the lowest Akaike information criterion and was used in the subsequent repeated measures multivariable models. To explore the effect of heat stress and maternal heat strain on the fetus, we used two multivariable repeated measures models with FHR (model A, linear regression) and fetal strain (model B, logistic regression) as outcomes. All variables were decided a priori on the basis of biological plausibility and directed acyclic graphs (appendix pp 13–14). Model 1 shows the total effect of heat stress on fetal strain or FHR: wherein fetal strain or fetal heart rate for individual i at time j (Y) and heat stress exposure for individual i at time j are represented. Model 1 gives the estimate of effect (model A) and the odds ratio (OR; model B) for each 1°C increase in heat stress on fetal strain to give the total effect of heat stress. Model 2 gives the direct effect of heat stress on fetal strain while controlling for maternal heat strain: wherein FHR or fetal strain for individual i at time j (Y), UTCI or WBGT for individual i at time j (heat stress), PSIMOD of individual i at time j (heat strain), estimation of cardiovascular fitness determined by distance travelled in standardised 6 min walk test for individual i at time j (fitness), and measurement of body fat (as BMI is not useful in pregnancy) for individual i at time j (% fat mass) are represented. Model 2 gives the estimate of effect (model A) and the OR (model B) for each 1°C increase in heat stress on fetal strain, controlling for maternal heat strain. This model estimates the effects of heat stress on fetal strain due to other mechanisms outside of maternal heat strain. Model 3 gives the direct effect of maternal heat strain on fetal strain while controlling for heat stress, cardiac fitness, percentage of fat mass, and gestational age: wherein FHR or fetal strain for individual i at time j (Y), UTCI or WBGT for individual i at time j (heat stress), PSIMOD of individual i at time j (heat strain), estimation of cardiovascular fitness determined by distance travelled in standardised 6 min walk test for individual i at time j (fitness), and measurement of body fat (as BMI is not useful in pregnancy) for individual i at time j (% fat mass) are represented. Full details of all models and analysis code can be found in the appendix (pp 19–22). The final models were assessed for violation of model assumptions by assessing the linearity of residuals, homoscedasticity by Levene’s Test, and the normal distribution of residuals. The funder of the study had no role in study design, data collection, data analysis, data interpretation, or writing of the report.