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接受卵巢癌化疗的女性个体化步行干预的安全性、可行性和效果:一项初步研究。

Safety, feasibility and effects of an individualised walking intervention for women undergoing chemotherapy for ovarian cancer: a pilot study.

机构信息

School of Public Health, Queensland University of Technology, Brisbane, Australia.

出版信息

BMC Cancer. 2011 Sep 8;11:389. doi: 10.1186/1471-2407-11-389.

Abstract

BACKGROUND

Exercise interventions during adjuvant cancer therapy have been shown to increase functional capacity, relieve fatigue and distress and may assist rates of chemotherapy completion. These studies have been limited to breast, gastric and mixed cancer groups and it is not yet known if a similar intervention is even feasible among women with ovarian cancer. We aimed to assess safety, feasibility and potential effect of a walking intervention in women undergoing chemotherapy for ovarian cancer.

METHODS

Women newly diagnosed with ovarian cancer were recruited to participate in an individualised walking intervention throughout chemotherapy and were assessed pre- and post-intervention. Feasibility measures included session adherence, compliance with exercise physiologist prescribed walking targets and self-reported program acceptability. Changes in objective physical functioning (6-minute walk test), self-reported distress (Hospital Anxiety and Depression Scale), symptoms (Memorial Symptom Assessment Scale - Physical) and quality of life (Functional Assessment of Cancer Therapy - Ovarian) were calculated, and chemotherapy completion and adverse intervention effects recorded.

RESULTS

Seventeen women were enrolled (63% recruitment rate). Mean age was 60 years (SD = 8 years), 88% were diagnosed with FIGO stage III or IV disease, 14 women underwent adjuvant and three neo-adjuvant chemotherapy. On average, women adhered to > 80% of their intervention sessions and complied with 76% of their walking targets, with the majority walking four days a week at moderate intensity for 30 minutes per session. Meaningful improvements were found in physical functioning, physical symptoms, physical well-being and ovarian cancer-specific quality of life. Most women (76%) completed ≥85% of their planned chemotherapy dose. There were no withdrawals or serious adverse events and all women reported the program as being helpful.

CONCLUSIONS

These positive preliminary results suggest that this walking intervention for women receiving chemotherapy for ovarian cancer is safe, feasible and acceptable and could be used in development of future work.

TRIAL REGISTRATION

ACTRN12609000252213.

摘要

背景

辅助癌症治疗期间的运动干预已被证明可以提高功能能力、缓解疲劳和痛苦,并可能有助于提高化疗完成率。这些研究仅限于乳腺癌、胃癌和混合癌症群体,目前尚不清楚这种干预措施是否在卵巢癌女性中也是可行的。我们旨在评估在接受卵巢癌化疗的女性中进行步行干预的安全性、可行性和潜在效果。

方法

新诊断为卵巢癌的女性被招募参与整个化疗期间的个体化步行干预,并在干预前后进行评估。可行性措施包括参与度、遵守运动生理学家规定的步行目标以及自我报告的方案可接受性。计算了客观身体功能(6 分钟步行测试)、自我报告的困扰(医院焦虑和抑郁量表)、症状(纪念症状评估量表-身体)和生活质量(癌症治疗功能评估-卵巢)的变化,并记录了化疗完成情况和不良干预效果。

结果

共纳入 17 名女性(招募率为 63%)。平均年龄为 60 岁(标准差=8 岁),88%的女性被诊断为 FIGO 分期 III 或 IV 期疾病,14 名女性接受了辅助化疗,3 名女性接受了新辅助化疗。平均而言,女性坚持了超过 80%的干预课程,并遵守了 76%的步行目标,大多数女性每周坚持 4 天、中等强度、每次 30 分钟的步行运动。身体功能、身体症状、身体幸福感和卵巢癌特异性生活质量都有了显著改善。大多数女性(76%)完成了≥85%的计划化疗剂量。没有退出或严重不良事件,所有女性都报告该方案很有帮助。

结论

这些初步的积极结果表明,对于接受卵巢癌化疗的女性,这种步行干预是安全、可行和可接受的,可用于未来的研究。

试验注册

ACTRN12609000252213。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/727d/3189191/1e1020aa21cd/1471-2407-11-389-1.jpg

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