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Accepted for/Published in: JMIR Cancer

Date Submitted: Sep 15, 2025
Open Peer Review Period: Sep 15, 2025 - Nov 10, 2025
Date Accepted: Sep 18, 2026
(closed for review but you can still tweet)

The final, peer-reviewed published version of this preprint can be found here:

Symptom Management Following Radioactive Iodine Treatment in Adults With Thyroid Cancer: Usability Evaluation and Proof-of-Concept Study

Carr A, Jenkins AM, Gómez V, Lorenzo JA, Moclair R, Pocchia J, Gandhi D, Miller K, Graves KD, Jonklaas J

Symptom Management Following Radioactive Iodine Treatment in Adults With Thyroid Cancer: Usability Evaluation and Proof-of-Concept Study

JMIR Cancer 2026;12:e84151

DOI: 10.2196/84151

PMID: 42868528

Symptom Management Following Radioactive Iodine Treatment in Adults with Thyroid Cancer: Usability Evaluation and Proof-of-Concept

  • Alaina Carr; 
  • Angela M Jenkins; 
  • Valeria Gómez; 
  • Janine Alexandria Lorenzo; 
  • Ryan Moclair; 
  • James Pocchia; 
  • Devansh Gandhi; 
  • Kristen Miller; 
  • Kristi D Graves; 
  • Jacqueline Jonklaas

ABSTRACT

Background:

Thyroid cancer is often labeled a “good cancer” due to high survival rates. However, many patients diagnosed with differentiated thyroid cancer (DTC) treated with radioactive iodine (RAI) experience short- and long-term symptoms as a result of treatment. These include salivary dysfunction, dry mouth, dry eyes, and nausea. Despite these challenges, patients report limited knowledge and unmet informational needs regarding RAI symptoms and symptom management. Evidenced-based, patient-centered education to support symptom management during DTC survivorship is needed. Our team developed RAI Support, a prototype of a four-week web-based intervention for RAI symptom management among DTC survivors.

Objective:

Evaluate the usability of the RAI Support intervention among DTC survivors who completed RAI treatment and assess intervention signals of change for RAI symptom burden, self-efficacy for managing chronic symptoms, informational needs, global physical and mental health, and health-related quality of life (HRQOL).

Methods:

We conducted a longitudinal usability testing study with eight participants over a 4-week period. At baseline (T1), participants completed an online survey and a 90-minute virtual usability testing session. During usability testing sessions, study staff used a think-aloud protocol to elicit feedback on the content, language, and visual appeal of the prototype across five tasks. Participants also completed the System Usability Scale (SUS). Participants were encouraged to continue using the intervention over the 4-week period, during which usage data was recorded. A follow-up post-assessment (T2) was completed at the end of the four-week period of home use. Survey outcomes included RAI symptom burden, self-efficacy for managing chronic symptoms, informational needs, global physical and mental health, and HRQOL.

Results:

Among the eight DTC survivors post-RAI (Mage = 45, SD = 8.2), the mean SUS score was 88.1 (SD = 8.7) indicating above-average usability. All participants effectively completed each task, with ease of use ranging from 100% to 87.5% and error rates ranging from 0 to 25%. Clinically significant pre- to post- intervention r effect sizes were found for improved self-efficacy, global mental health, and HRQOL (rrange = 0.15-0.45).

Conclusions:

DTC survivors reported above average usability of the RAI Support prototype and completed each task successfully. Variability in error rates and ease of use suggest that refinements are needed to further optimize usability and patient engagement. RAI Support also shows promise in improving DTC survivors’ self-efficacy in managing symptoms, global mental health and HRQOL. Findings support future pilot testing.


 Citation

Please cite as:

Carr A, Jenkins AM, Gómez V, Lorenzo JA, Moclair R, Pocchia J, Gandhi D, Miller K, Graves KD, Jonklaas J

Symptom Management Following Radioactive Iodine Treatment in Adults With Thyroid Cancer: Usability Evaluation and Proof-of-Concept Study

JMIR Cancer 2026;12:e84151

DOI: 10.2196/84151

PMID: 42868528

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