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Objective <p>Family-based treatment (FBT) is the treatment of choice for adolescent anorexia nervosa (AN). Although effective, caregivers often experience significant emotional strain, uncertainty, and distress whilst undergoing FBT. This study aims to explore how parents, adolescents, and clinicians experience challenges of family life and caregiving during FBT.</p> Method <p>A qualitative design was employed using focus groups with parents (<i>N</i> = 10), individuals recovered from adolescent-onset AN (<i>N</i> = 4), and clinicians (<i>N</i> = 8). Reflexive thematic analysis was applied to identify themes.</p> Results <p>Four overarching themes were identified: 1) AN as an intrusive force disrupting family life, 2) shared experiences of guilt, doubt, and isolation, 3) the evolving parental role within treatment, and 4) the reorganization of family dynamics around the illness. Parents described significant ambivalence toward treatment responsibilities, while adolescents struggled with isolation. Clinicians noted discrepancies in how different stakeholders understood and engaged with treatment.</p> Conclusions <p>Our findings highlight the importance of addressing both the practical and emotional aspects of caregiving to enhance treatment outcomes, as FBT remains an essential intervention for adolescent AN. Further research should investigate ways to strengthen caregiver empowerment and mitigate distress while maintaining the core principles of FBT.</p>

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Family life and caregiving during family-based treatment (FBT) for anorexia nervosa: parent, patient, and clinician perspectives

  • 期刊论文

  • 出版模式：

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  • 发表日期：

    2025年10月6日

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  • Dorthe Waage,
  • Anne Bryde,
  • Mette Bentz,
  • Nadia Micali

摘要

Objective

Family-based treatment (FBT) is the treatment of choice for adolescent anorexia nervosa (AN). Although effective, caregivers often experience significant emotional strain, uncertainty, and distress whilst undergoing FBT. This study aims to explore how parents, adolescents, and clinicians experience challenges of family life and caregiving during FBT.

Method

A qualitative design was employed using focus groups with parents (N = 10), individuals recovered from adolescent-onset AN (N = 4), and clinicians (N = 8). Reflexive thematic analysis was applied to identify themes.

Results

Four overarching themes were identified: 1) AN as an intrusive force disrupting family life, 2) shared experiences of guilt, doubt, and isolation, 3) the evolving parental role within treatment, and 4) the reorganization of family dynamics around the illness. Parents described significant ambivalence toward treatment responsibilities, while adolescents struggled with isolation. Clinicians noted discrepancies in how different stakeholders understood and engaged with treatment.

Conclusions

Our findings highlight the importance of addressing both the practical and emotional aspects of caregiving to enhance treatment outcomes, as FBT remains an essential intervention for adolescent AN. Further research should investigate ways to strengthen caregiver empowerment and mitigate distress while maintaining the core principles of FBT.