Adaptation of the Patient Reported Outcome Measurement Information System (PROMIS) tool for childhood cancer in India: A qualitative study. Issue 10 (25th August 2022)

• Record Type: Journal Article
• Authors: Sasi, Archana; Ganguly, Shuvadeep; Sharma, Shubhangi; Singh, Ritika; Verma, Vasudha; Bisht, Reema; Kalra, Devanshi; Satapathy, Sujata; Bakhshi, Sameer
• Is Part Of: Psycho-oncology. Volume 31:Issue 10(2022)
• Page Start: 1671
• Page End: 1680
• Publication Date: 2022-08-25
• Subjects: childhood cancer -- patient‐reported outcomes -- pediatric cancer -- pediatric oncology -- quality of life; Cancer -- Psychological aspects -- Periodicals; Cancer -- Social aspects -- Periodicals; Neoplasms -- psychology -- Periodicals; 616.9940019
• DOI: 10.1002/pon.6017
• Languages: English
• ISSNs: 1057-9249

Abstract

Abstract: Background: To fill the gap in patient‐reported outcome (PRO) assessment in children with cancer in India, we planned to adapt domains from the HealthMeasures Patient Reported Outcomes Measurement Information System (PROMIS) tool. This study attempted to identify and pool outcomes relevant to children with cancer and their caregivers in Northern India. Methods: The study was qualitative and conducted through focussed group discussions (FGDs) and in‐depth interviews of children with cancer and their caregivers. Content analysis of transcripts from the sessions was done. The collected themes were collated with existing item banks of the PROMIS tool and new concepts unique to our population were compiled. Results: A set of three FGDs and 14 interviews each for children and their caregivers were conducted. Following content analysis, 121 themes were identified including 10 new concepts. Themes pertaining to the physical domain were cited most. The theme distribution across the three domains was similar among children and caregivers. In the survivor cohort, the relative frequency of mention of psychological and social themes was higher compared to the whole cohort. Themes pertaining to mobility, cognitive dysfunction and peer relationships were more common among survivors. Conclusions: This qualitative study in children with cancer and their caregivers in India has facilitated a better understanding of the issues pertaining to cancer care that are of most importance to its stake holders. The themes collected may be used to formulate a PRO tool uniquely tailored for use in this population.