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限时进食改善癌症幸存者持续存在的癌症相关疲劳:一项随机对照试验。

Time-restricted eating to address persistent cancer-related fatigue among cancer survivors: a randomized controlled trial.

作者信息

Kleckner Amber S, Clingan Carin L, Youngblood Shari M, Kleckner Ian R, Quick Lauren, Elrod Rebecca D, Zhu Shijun, Manoogian Emily N C, Panda Satchidananda, Badros Ashraf Z, Emadi Ashkan

机构信息

Department of Pain and Translational Symptom Science, University of Maryland School of Nursing, 655 W. Lombard Ave., 7th Floor, Baltimore, MD, 21201, USA.

Greenebaum Comprehensive Cancer Center, 22 S. Greene St., Baltimore, MD, 21201, USA.

出版信息

Support Care Cancer. 2025 Apr 5;33(4):353. doi: 10.1007/s00520-025-09394-w.

Abstract

PURPOSE

Time-restricted eating (TRE) helps regulate rest-activity rhythms, blood glucose, and other diurnally regulated energetics processes, which may have implications for persistent fatigue. In a randomized controlled trial, we tested the effects of TRE vs. control on fatigue in cancer survivorship.

METHODS

Adult cancer survivors were recruited who were 2 months to 2 years post-treatment and reported moderate to severe fatigue. Participants were randomized 1:1, TRE:control, and all received individualized nutrition counseling. The TRE group self-selected a 10-h eating window for 12 weeks. At baseline, week 6, and week 12, participants were asked to log eating instances, complete the Functional Assessment of Chronic Illness Therapy-Fatigue questionnaire (FACIT-F, higher score = less fatigue), and wear an actigraph and continuous glucose monitor.

RESULTS

Thirty participants completed baseline assessments and were randomized (77% female, 53% Black/African American, 43% White, 7% Hispanic; 54.1 ± 14.7 years old; 87% with blood cancer); 25 completed 12-week assessments. TRE led to a meaningful reduction in fatigue at week 12 controlling for baseline levels (change in FACIT-F fatigue subscale = 0.0 ± 5.4 for control, 4.1 ± 5.7 for TRE, p = 0.11, effect size (ES) = 0.70; clinically meaningful threshold = 3.0 points). Glucose parameters (e.g., average interstitial glucose, average fasting glucose) tended to be lower, and rest-activity rhythms tended to indicate more regularity for those in the TRE vs. control group at weeks 6 and 12, though differences were not statistically significant (p > 0.19).

CONCLUSIONS

A 12-week, nutritionist-led TRE program led to less fatigue than control. Continued study of TRE patterns are warranted to optimize this eating pattern and address persistent cancer-related fatigue.

TRIAL REGISTRATION

ClinicalTrials.gov Identifier: NCT05256888.

摘要

目的

限时进食(TRE)有助于调节休息-活动节律、血糖和其他昼夜调节的能量代谢过程,这可能对持续性疲劳有影响。在一项随机对照试验中,我们测试了TRE与对照相比对癌症幸存者疲劳的影响。

方法

招募治疗后2个月至2年且报告有中度至重度疲劳的成年癌症幸存者。参与者按1:1随机分组,TRE组:对照组,所有参与者均接受个性化营养咨询。TRE组自行选择10小时的进食窗口,为期12周。在基线、第6周和第12周,要求参与者记录进食情况,完成慢性病治疗功能评估-疲劳问卷(FACIT-F,分数越高=疲劳越少),并佩戴活动记录仪和连续血糖监测仪。

结果

30名参与者完成了基线评估并被随机分组(77%为女性,53%为黑人/非裔美国人,43%为白人,7%为西班牙裔;54.1±14.7岁;87%患有血癌);25名完成了12周评估。在控制基线水平的情况下,TRE在第12周时使疲劳有了显著降低(FACIT-F疲劳子量表变化:对照组为0.0±5.4,TRE组为4.1±5.7,p = 0.11,效应量(ES)= 0.70;临床意义阈值 = 3.0分)。在第6周和第12周,与对照组相比,TRE组的葡萄糖参数(如平均组织间液葡萄糖、平均空腹血糖)往往更低,休息-活动节律往往更规律,尽管差异无统计学意义(p > 0.19)。

结论

由营养师指导的为期12周的TRE方案比对照组导致的疲劳更少。有必要继续研究TRE模式,以优化这种饮食模式并解决持续性癌症相关疲劳问题。

试验注册

ClinicalTrials.gov标识符:NCT05256888。

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