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Experiences Using Nonpharmacological Interventions for Chronic Fatigue: A Focus Group Study of Long-Term Survivors of Young Adult Cancers With Fatigue.
Stub, Trine; Mathisen, Marleen; Thorsen, Lene; Kiserud, Cecilie E; Lie, Hanne C.
Affiliation
  • Stub T; NAFKAM-Norway's National Research Center in Complementary and Alternative Medicine, Faculty of Health Science, Department of Community Medicine, UiT, The Arctic University of Norway, Tromsø, Norway.
  • Mathisen M; Department of Behavioural Sciences in Medicine, Institute of Basic Medical Sciences in Medicine, Faculty of Medicine, University of Oslo, Oslo, Norway.
  • Thorsen L; Department of Oncology, Division of Cancer Medicine, Oslo University Hospital, Oslo, Norway.
  • Kiserud CE; Department of Oncology, Division of Cancer Medicine, Oslo University Hospital, Oslo, Norway.
  • Lie HC; Department of Behavioural Sciences in Medicine, Institute of Basic Medical Sciences in Medicine, Faculty of Medicine, University of Oslo, Oslo, Norway.
Cancer Rep (Hoboken) ; 7(9): e2139, 2024 Sep.
Article in En | MEDLINE | ID: mdl-39233646
ABSTRACT

BACKGROUND:

Cancer-related fatigue is a common and distressing late effect of cancer that can persist for decades after treatment completion. Although negatively affecting survivors' quality of life, few, if any, efficacious interventions for persistent, or chronic, fatigue exist.

AIMS:

To inform future interventions, we explored how long-term, young adult cancer survivors (YACSs) with chronic fatigue live with, and manage their fatigue over time, including their experiences with nonpharmacological interventions (NPIs) for chronic fatigue. METHODS AND

RESULTS:

We conducted a qualitative focus group study with 15 YACSs (13 women) with chronic fatigue, on average 7.3 years post-diagnosis. The YACS were identified and recruited through a nationwide health survey of cancer survivors (the NOR-CAYACS study). Systematic content analysis was used to identify recurrent themes. Analysis revealed five themes (1) manifestation of fatigue, detailing chronic fatigue experiences; (2) impact on daily life, highlighting the necessity to balance rest and activity, affecting relationships; (3) NPIs, where walks in nature were notably beneficial; (4) barriers to fatigue management, including energy deficits, treatment-related bodily changes, and self-care prioritization challenges; (5) facilitators to fatigue management, emphasizing the need for regular breaks, self-care practices, and the importance of fatigue management education.

CONCLUSION:

This study offers novel insights into the lived experiences of YACSs with chronic fatigue, a subject scarcely examined in prior research. Our findings highlight the significant impact of chronic fatigue and the individualized strategies YACSs use to cope. The research emphasizes the need for personalized interventions to support chronic fatigue management, marking a critical step forward in addressing this often-overlooked issue in survivorship care. Future research should focus on tailored approaches to improve YACSs' quality of life.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Quality of Life / Focus Groups / Qualitative Research / Cancer Survivors / Neoplasms Limits: Adult / Female / Humans / Male Language: En Journal: Cancer Rep (Hoboken) Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Quality of Life / Focus Groups / Qualitative Research / Cancer Survivors / Neoplasms Limits: Adult / Female / Humans / Male Language: En Journal: Cancer Rep (Hoboken) Year: 2024 Document type: Article