Evidence map›Paper›PMID 32990882›Full record

Trial reportQuality of life research : an international journal of quality of life aspects of treatment, care and rehabilitation2021

A randomised online experimental study to compare responses to brief and extended surveys of health-related quality of life and psychosocial outcomes among women with breast cancer.

Kerry Ettridge, Joanna Caruso, David Roder, Ivanka Prichard, Katrine Scharling-Gamba, Kathleen Wright, Caroline Miller

Abstract readRandomized Controlled Trial
PubMed Publisher
In one paragraph

Trial report in Quality of life research : an international journal of quality of life aspects of treatment, care and rehabilitation, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
–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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Methods to increase response to postal and electronic questionnaires.The Cochrane database of systematic reviews · 2023
    Pooled it
  2. Article
  3. Article
  4. Article
  5. Administering selected subscales of patient-reported outcome questionnaires to reduce patient burden and increase relevance: a position statement on a modular approach.Quality of life research : an international journal of quality of life aspects of treatment, care and rehabilitation · 2024
    Article
  6. Review
  7. Review
  8. Review
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

7 authors.

Kerry EttridgeSouth Australian Health and Medical Research Institute, North Terrace, Adelaide, SA, Australia. Kerry.ettridge@sahmri.com.ORCID http://orcid.org/0000-0001-7928-9692
Joanna CarusoSouth Australian Health and Medical Research Institute, North Terrace, Adelaide, SA, Australia.
David RoderUniversity of South Australia, Adelaide, SA, Australia.ORCID http://orcid.org/0000-0001-6442-4409
Ivanka PrichardCaring Futures Institute, Flinders University, Adelaide, SA, Australia.ORCID http://orcid.org/0000-0001-8892-9129
Katrine Scharling-GambaSouth Australian Health and Medical Research Institute, North Terrace, Adelaide, SA, Australia.
Kathleen WrightSouth Australian Health and Medical Research Institute, North Terrace, Adelaide, SA, Australia.ORCID http://orcid.org/0000-0002-6269-8729
Caroline MillerUniversity of Adelaide, Adelaide, SA, Australia.ORCID http://orcid.org/0000-0001-9723-8047

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeCollecting patient-reported outcomes is important in informing the well-being of women with breast cancer. Consumer perceptions are important for successful implementation of monitoring systems, but are rarely formally assessed. We compared reactions to two different surveys (assessing psychosocial outcomes and/or Health-related Quality of Life (HrQoL) outcomes) among Australian women with breast cancer.

methodsWomen (18 + years) within 5 years diagnosis of breast cancer were randomly allocated to complete one of two online surveys: (i) minimum HrQoL measures or (ii) minimum HrQoL measures plus psychosocial outcomes (body image, depression, anxiety stress, fear of cancer recurrence, decisional difficulties and unmet need). Participants completed questions regarding their perceptions of the survey, including qualitative feedback.

resultsData were available for 171 participants (n

conclusionsAssessment of HrQoL and psychosocial outcomes was well received by consumers. Results alleviate concern regarding possible patient burden imposed by longer more in-depth surveys. The importance placed on assessment brevity should not outweigh the need to assess outcomes that consumers consider important.

Indexed as

AdultAgedBreast NeoplasmsFemaleHumansInternetMiddle AgedPsychologyQuality of LifeSurveys and QuestionnairesBreast cancerConsumer perspectivesHealth-related quality of life (HrQoL)Patient-reported outcome measures (PROMs)Psychosocial

Identifiers

What OpenQuestion holds

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Registered trials

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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.