Aims
Women affected by ovarian cancer (OC) face an uncertain prognosis and report high fear of cancer recurrence (FCR). This pilot randomised wait-list controlled trial aimed to evaluate the acceptability, feasibility and safety of iConquerFear, a self-guided online FCR intervention for OC survivors.
Methods
We recruited women (≥18 years) post-treatment for stage I-III OC via Ovarian Cancer Australia from October-December 2022. Eligible women were randomised to access iConquerFear immediately (intervention) or after 8 weeks (wait-list control). Outcomes assessed were: feasibility – ≥50% of women expressing interest access iConquerFear, and ≥50% of those complete ≥3/5 therapeutic modules; acceptability – mean post-intervention satisfaction rating ≥75/100; safety – ≤5% withdrawals due to worsened FCR/distress from iConquerFear. Semi-structured interviews with a sub-sample explored factors influencing iConquerFear uptake, engagement, and benefit.
Results
90 women expressed interest, 62 completed eligibility screening; 58 (64%) were randomised (intervention n=27, wait-list n=31). Most participants had stage III OC (n=34, 59%); Mean FCR = 20/36 (SD=6.7). Of those randomised 27 (47%) accessed iConquerFear (13 intervention, 14 wait-list participants), and 59% completed ≥3/5 therapeutic modules. Post-randomisation, 19 women (33%) withdrew, 8 (14%) due to recurrence, 3 (5%) due to increased FCR/distress. Mean post-intervention satisfaction (n=25) was 80/100 (SD=26). Thematic analysis of 14 interviews generated six themes: 1) Varying perspectives on timing and method of recommending iConquerFear, 2) Participant factors influencing engagement, 3) Website factors influencing engagement, 4) Need to balance flexibility of self-guided online programs and opportunities for personal connection, 5) Desire for deeper, more specific discussions of lived experiences, 6) Personal impact of iConquerFear.
Conclusions
Feasibility of iConquerFear was limited by low uptake. Women who accessed iConquerFear generally completed the recommended dose and were satisfied. More tailored website content and greater personal support are needed, particularly in cases of increased distress during iConquerFear use.