Testing a Smartphone-Based Intervention Targeting Anxiety Sensitivity Among Women Presenting for Emergency Care After Sexual Assault: Pilot Randomized Controlled Trial

Clinical Snapshot

Key Findings

• P Value: Statistically significant at 6 months (specific values not provided)

• Effect Size: Not reported in abstract

• Primary Outcome: Anxiety sensitivity and PTSD symptom reduction

• Nnt Or Sensitivity: Not calculable from available data

• Confidence Interval: Not reported

Clinical Application

Moderate - recruitment and retention feasible but intervention completion remains challenging Relevant to Australian emergency departments and sexual assault services; could complement existing CASA (Centres Against Sexual Assault) programs and align with trauma-informed care principles Women sexual assault survivors presenting to emergency departments with high anxiety sensitivity

Abstract

BACKGROUND: Anxiety sensitivity (AS), defined as the fear of anxious arousal, is a promising therapeutic target for reducing posttraumatic stress disorder (PTSD) symptom development after trauma exposure. Initial research suggests that smartphone-based AS interventions may be acceptable to sexual assault survivors at risk for PTSD symptoms and effective for symptom reduction, but only small one-arm proof-of-concept studies have been conducted. OBJECTIVE: The goal of this study was to extend prior proof-of-concept work by conducting a pilot randomized controlled trial. The aims were to evaluate intervention efficacy, AS and PTSD symptom change, the acceptability and credibility of a control intervention, and the feasibility of a larger randomized controlled trial. METHODS: A total of 60 women with high AS presenting for emergency care after sexual assault were recruited and randomized to either the AS intervention or a control condition, and they were followed up with for over 6 months via remote self-report questionnaires. RESULTS: The findings indicated that the study population is at risk and in need of intervention: 88.8% (40/45) and 80.6% (29/36) of women sexual assault survivors in the sample met the criteria for probable PTSD at 7 weeks and 6 months post assault, respectively. Most (16/27, 59.3%) individuals receiving the AS intervention who completed it rated it as acceptable (eg, 18/21, 85.7% reported that the treatment was helpful). Early within-group reductions were not statistically significant, but by month 6, statistically significant reductions in AS and PTSD symptoms were observed in both conditions. Recruitment and retention data supported the feasibility of the study design, although some suggestions were noted for future research (eg, improving intervention and ecological momentary assessment compliance). CONCLUSIONS: This pilot study replicated the proof of concept and acceptability of a novel smartphone-based intervention targeting AS delivered to women sexual assault survivors presenting to emergency care. Intervention completion was in line with or better than traditional therapy but remained a challenge. Our selected control condition demonstrated a larger effect than expected, and we were unable to track its initiation or completion, causing difficulty in drawing conclusions. Overall, the results highlight the need for additional research.

References

1. 1.Short, N. A., Deguzman-Lucero, R., Weese, R., Chisam, N., Black, J., Serrano, K., & McLean, S. (2026). Testing a smartphone-based intervention targeting anxiety sensitivity among women presenting for emergency care after sexual assault: Pilot randomized controlled trial. JMIR Formative Research. https://doi.org/10.2196/86612