# Ecological momentary assessments for patients with hereditary angioedema: a feasibility and acceptability controlled study

**Authors:** Monica Parati, Luca Ranucci, Azzurra Cesoni Marcelli, Lorenza Chiara Zingale, Beatrice De Maria, Clara Gino, Aida Zulueta, Riccardo Sideri, Alessandra Gorini, Francesca Perego

PMC · DOI: 10.3389/fdgth.2025.1693550 · Frontiers in Digital Health · 2026-01-12

## TL;DR

This study shows that using real-time surveys to monitor emotions is practical and well-received by patients with a rare condition called hereditary angioedema.

## Contribution

The study demonstrates the feasibility and acceptability of Ecological Momentary Assessment (EMA) in a rare disease population.

## Key findings

- EMA had high recruitment, response, and completion rates in both HAE patients and healthy controls.
- EMA was rated as acceptable and helpful by HAE participants, with no significant differences in completion time between groups.
- The results suggest that rare disease status does not hinder the use of EMA for affect monitoring.

## Abstract

Hereditary angioedema (HAE) is a rare disease imposing a significant quality of life burden. Affect monitoring via Ecological Momentary Assessment (EMA) could offer personalized psychological support by collecting repeated, ecological data in real-life, overcoming the limitations of traditional methods. This study assessed the feasibility and acceptability of an EMA protocol for affect monitoring in HAE patients vs. healthy controls (CTR).

HAE patients and CTR were recruited for a 16-week EMA study. Participants received weekly EMA surveys assessing affect via REDCap™. Feasibility was evaluated through recruitment, response, and completion rates. Acceptability was assessed via a post-study questionnaire through a visual analogue scale ranging from 1 to 100.

Twenty-eight Caucasian subjects were contacted, 12 HAE [median age: 50 (22) years, 5 males] and 14 CTR [age: 30 (32) years, 6 males] agreed to participate, resulting in a recruitment rate of 93%. Response and completion rates were ≥92% and ≥96% respectively in both groups. Completion time was brief and did not differ between groups [HAE: 1′ 28″ (29″) vs. CTR: 1′ 15′ (15″), P = 0.274]. The protocol was considered acceptable by both groups [HAE: rate 83.5 (18.8) vs. CTR: 72.0 (13.0), p = 0.27] with HAE rating the experience as helpful [79 (39.8)] and thought-provoking [67 (33)].

EMA is a highly feasible and acceptable method for affect monitoring in HAE. The presence of a rare disease does not appear to be a barrier to its application, supporting its use in this clinical setting.

## Linked entities

- **Diseases:** hereditary angioedema (MONDO:0019623)

## Full-text entities

- **Diseases:** HAE (MESH:D054179)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12833764/full.md

## References

43 references — full list in the complete paper: https://tomesphere.com/paper/PMC12833764/full.md

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Source: https://tomesphere.com/paper/PMC12833764