Managing fear of cancer recurrence: a qualitative comparison of coping process among Chinese cancer survivors with nonclinical, subclinical, and clinically-significant fear of cancer recurrence


Grant Data
Project Title
Managing fear of cancer recurrence: a qualitative comparison of coping process among Chinese cancer survivors with nonclinical, subclinical, and clinically-significant fear of cancer recurrence
Principal Investigator
Dr Ng, Wing Lam   (Principal Investigator (PI))
Co-Investigator(s)
Dr Chan Wing Lok Wendy   (Co-Investigator)
Dr Foo Chi Chung   (Co-Investigator)
Dr Tang Wei Chun Julia   (Co-Investigator)
Professor Kwong Ava   (Co-Investigator)
Professor Ng Simon Siu-man   (Co-Investigator)
Professor Fielding Richard   (Co-Investigator)
Dr Lam Wendy Wing Tak   (Co-Investigator)
Duration
12
Start Date
2022-01-08
Amount
522083
Conference Title
Managing fear of cancer recurrence: a qualitative comparison of coping process among Chinese cancer survivors with nonclinical, subclinical, and clinically-significant fear of cancer recurrence
Presentation Title
Keywords
Breast cancer, Cancer survivoship, Colorectal cancer, Coping, Fear of cancer recurrence, Psycho-oncology
Discipline
Others - Medicine, Dentistry and Health
HKU Project Code
18191511
Grant Type
Health and Medical Research Fund - Full Grant
Funding Year
2020
Status
On-going
Objectives
(1) Objectives: The aims of this qualitative study are to (1) identify coping strategies used to manage fear of cancer recurrence (FCR) among Chinese cancer survivors; (2) compare coping strategies used among survivors with nonclinical, subclinical, and clinically-significant FCR; and (3) explore factors influencing the coping process of FCR among survivors with nonclinical, subclinical, and clinically-significant FCR. (2) Hypothesis to be tested: NA (3) Design and subjects: Using qualitative study design, this study will include Cantonese- or Mandarin-speaking Chinese cancer survivors with non-metastatic breast or colorectal cancer survivors who have recently completed adjuvant treatment (except hormonal therapy) from the public clinical oncology centres, and will stratify them into nonclinical, subclinical and clinically-significant FCR for comparison. A total of 45 participants will be recruited with 15 in each FCR status. (4) Instruments: Fear of cancer recurrence inventory-short form (FCRI-SF) will be used for FCR screening. FCRI-SF scores of < 13, 13 to 21, and ≥ 22 indicate nonclinical, subclinical and clinically-significant FCR cases, respectively. Individual face-to-face semi-structured interview will be used to collect narrative data. (5) Intervention: NA (6) Main outcome measures: Narrative data (7) Data analysis: Grounded theory approach will be employed for data analysis. (8) Expected results: The findings of the proposed study will enable us to have a better understanding of the variance in FCR seen in cancer survivors that allows for potential early identification and refinement of the existing intervention for preventing FCR worsening.