Evidence map›Paper›PMID 41642626›Full record

Trial reportJAMA network open2026

Self-Acupressure for Fatigue in Patients Surviving Ovarian Cancer: A Randomized Clinical Trial.

Suzanna M Zick, Dongru Chen, Richard E Harris, Grant Kruger, Amy Runyon, Ananda Sen, Sara Snyder, Celeste Leigh Pearce

Registry-linked trialAbstract readRandomized Controlled TrialClinical Trial, Phase III
In one paragraph

Trial report in JAMA network open, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03763838 (Acupressure for Fatigue in Ovarian Cancer Survivors), which is not on this map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT03763838 nacompletednot on this map

Acupressure for Fatigue in Ovarian Cancer Survivors

TypeinterventionalSponsorUniversity of Michigan Rogel Cancer CenterRan2019 to 2024Enrolled171ConditionsFatigue, Ovarian CancerArmsAcupressure, Sham acupressure, Standard of Care
3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Determining the feasibility of self-administered relaxing acupressure for fatigue among adolescent and young adult cancer survivors.Supportive care in cancer : official journal of the Multinational Association of Supportive Care in Cancer · 2026
    Trial
  2. Article
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors.

Suzanna M ZickDepartment of Family Medicine and Nutritional Sciences, University of Michigan, Ann Arbor.
Dongru ChenDepartment of Family Medicine, University of Michigan Medicine, Ann Arbor.
Richard E HarrisDepartment of Anesthesiology, University of Michigan, Ann Arbor.
Grant KrugerDepartment of Mechanical Engineering and Anesthesiology, University of Michigan Medicine, Ann Arbor.
Amy RunyonDepartment of Family Medicine, University of Michigan Medicine, Ann Arbor.
Ananda SenDepartment of Family Medicine and Biostatistics, University of Michigan Medicine, Ann Arbor.
Sara SnyderDepartment of Family Medicine, University of Michigan Medicine, Ann Arbor.
Celeste Leigh PearceDepartment of Epidemiology, University of Michigan, Ann Arbor.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Importance: Fatigue is a burdensome effect of ovarian cancer that is associated with poor sleep and quality of life. Self-acupressure is recommended in clinical guidelines but has substantial barriers to implementation. Use of a mobile app may address these barriers. Objective: To investigate whether 6 weeks of true self-acupressure (TSA), learned via a mobile app, improves cancer fatigue, sleep, and quality of life in women with ovarian cancer compared with sham self-acupressure (SSA) and usual care (UC) and whether changes are sustained during an 18-week washout period. Design, Setting, and Participants: This phase 3 single-blind randomized clinical trial was conducted from October 2019 to December 2023. Data collection ended in November 2024. Participants included ovarian cancer survivors who were fatigued (based on a Brief Fatigue Inventory [BFI] score ≥4) and who were recruited from tumor registries and social media. Intervention: Randomization (1:1:1) to 6 weeks of TSA or SSA, taught via mobile app, or UC. Main Outcomes and Measures: The primary outcome was the change in the BFI from baseline to week 6. Secondary analyses were the BFI score at week 24 and sleep disturbance (based on the Pittsburgh Sleep Quality Index) and quality of life (based on the Functional Assessment of Cancer Therapy-Ovarian) administered at baseline and at weeks 6, 12, and 24. Results: Among the 360 participants who were screened, 171 women were randomized (mean [SD] age, 56 [12] years). Of the 160 participants who were allocated to the arms, 53 (33.1%) received TSA, 56 (35.0%) received SSA, and 51 (31.9%) received UC. Of these, the proportion achieving a clinically normal fatigue level at the end of treatment was 58.5% for the TSA arm, 51.1% for the SSA arm, and 17.6% for the UC arm. At 6 weeks, the BFI change scores were significantly better in the TSA arm but not in the SSA arm when they were compared with the UC-only arm (TSA vs UC: adjusted mean difference, -1.23 [95% CI, -2.17 to -0.29] and SSA vs UC: adjusted mean difference, -0.91 [95% CI, -1.83 to 0.02]). TSA and SSA change scores did not differ significantly from one another. The relative benefit of self-acupressure compared with UC on fatigue persisted at 24 weeks (TSA vs UC: mean difference, -1.38 [95% CI, -2.36 to -0.41] and SSA vs UC: mean difference, -0.97 [95% CI, -1.93 to -0.02]). Neither TSA nor SSA was significantly different than UC or each other for sleep quality. Only TSA significantly improved quality of life vs UC (odds ratio, 2.85 [95% CI, 1.20 to 6.80]). Neither true nor sham self-acupressure led to any adverse events. Conclusions and Relevance: In this randomized clinical trial, TSA and SSA significantly reduced fatigue compared with UC, and these changes were both clinically meaningful and sustained. No impact was observed on sleep quality. Self-acupressure, taught via a mobile app, offered a safe and low-cost option for managing cancer fatigue. Trial registration: ClinicalTrials.gov Identifier: NCT03763838.

Indexed as

Cancer SurvivorsFatigueOvarian NeoplasmsSelf CareAgedFemaleHumansMiddle AgedMobile ApplicationsQuality of LifeSingle-Blind Method

Identifiers

PMID41642626
PMCPMC12878437

What OpenQuestion holds

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Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.