Evidence map›Paper›PMID 34870608›Full record

ArticleJMIR formative research2021

Patient-Reported Outcome Measure for Real-time Symptom Assessment in Women With Endometriosis: Focus Group Study.

Esther van Barneveld, Arianne Lim, Nehalennia van Hanegem, Lisa Vork, Alexandra Herrewegh, Mikal van Poll, Jessica Manders, Frits van Osch, Wilbert Spaans, Gommert van Koeveringe and 4 more

Open access · goldAbstract read
In one paragraph

Article in JMIR formative research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.8field-weighted citation impact, top 26% of its field
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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Review
  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

14 authors at 4 institutions in 1 country.

Esther van BarneveldDepartment of Gynaecology and Obstetrics, Maastricht University Medical Centre+, Maastricht, Netherlands.ORCID https://orcid.org/0000-0003-2801-8248
Arianne LimDepartment of Gynaecology and Obstetrics, Maastricht University Medical Centre+, Maastricht, Netherlands.ORCID https://orcid.org/0000-0002-5688-965X
Nehalennia van HanegemDepartment of Gynaecology and Obstetrics, University Medical Centre Utrecht, Utrecht, Netherlands.ORCID https://orcid.org/0000-0003-1394-0256
Lisa VorkDepartment of Internal Medicine, Division of Gastroenterology and Hepatology, Maastricht University Medical Centre+, Maastricht, Netherlands.ORCID https://orcid.org/0000-0001-7316-3191
Alexandra HerreweghDepartment of Urology, Maastricht University Medical Centre+, Maastricht, Netherlands.ORCID https://orcid.org/0000-0002-7306-5513
Mikal van PollMaastricht University, Maastricht, Netherlands.ORCID https://orcid.org/0000-0002-9937-0495
Jessica MandersMaastricht University, Maastricht, Netherlands.ORCID https://orcid.org/0000-0001-8315-4774
Frits van OschNUTRIM School of Nutrition and Translational Research in Metabolism, Maastricht University, Maastricht, Netherlands.ORCID https://orcid.org/0000-0003-4329-2560
Wilbert SpaansDepartment of Gynaecology and Obstetrics, Maastricht University Medical Centre+, Maastricht, Netherlands.ORCID https://orcid.org/0000-0002-3619-712X
Gommert van KoeveringeDepartment of Urology, Maastricht University Medical Centre+, Maastricht, Netherlands.ORCID https://orcid.org/0000-0003-2328-8265
Desiree VrijensDepartment of Urology, Maastricht University Medical Centre+, Maastricht, Netherlands.ORCID https://orcid.org/0000-0002-7596-1119
Joanna KruimelDepartment of Internal Medicine, Division of Gastroenterology and Hepatology, Maastricht University Medical Centre+, Maastricht, Netherlands.ORCID https://orcid.org/0000-0001-7102-1720
Marlies BongersDepartment of Gynaecology and Obstetrics, Maastricht University Medical Centre+, Maastricht, Netherlands.ORCID https://orcid.org/0000-0001-9276-9148
Carsten LeueSchool for Mental Health and Neuroscience (MeHNS), Maastricht University, Maastricht, Netherlands.ORCID https://orcid.org/0000-0003-1553-5705
Maastricht University Medical Centre · NLMaastricht University · NLRadboud University Nijmegen · NLUniversity Medical Center Utrecht · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSymptoms related to endometriosis have a significant impact on the quality of life, and symptoms often recur. The experience sampling method (ESM), a digital questioning method characterized by randomly repeated momentary assessments, has several advantages over traditionally used measurements, including the ability to assess the temporal relationship between variables such as physical, mental, and social factors.

objectiveThe aim of this study is to develop an ESM tool for patients with endometriosis to accurately measure symptoms and their course over time, allowing for personalized treatment and adequate monitoring of treatment efficacy in individual patients.

methodsOn the basis of international guidelines, items from validated questionnaires were selected through a literature review and during focus groups and multidisciplinary expert meetings. Data analysis was conducted using ATLAS.ti (ATLAS.ti Scientific Software Development GmbH). The feasibility and usability of the newly developed momentary assessment tool were tested for 28 consecutive days in 5 patients with endometriosis-related pain symptoms.

resultsMomentary assessment items contained questions concerning endometriosis symptoms, general somatic symptoms, psychological symptoms, contextual information, and the use of food and medication. A morning questionnaire on sleep and sexuality was included. In a pilot study, the patients considered the tool easy to use but time consuming. The average compliance rate of momentary assessments was 37.8% (106/280), with the highest completion rate during the first week (39/70, 56%). Therefore, it is advisable to use the ESM for a maximum of 7 days.

conclusionsA new digital tool for endometriosis symptom assessment was developed using the ESM, which may help overcome the limitations of current retrospective questionnaires. After validation and testing, future studies will be planned to evaluate the use of this tool in a clinical setting in order to propose a personalized treatment plan for women with endometriosis.

Indexed as

endometriosisexperience sampling methodfocus groupsmobile phonemomentary symptom assessmentnegative affectpatient-reported outcome measurepelvic painpositive affect

Identifiers

PMID34870608
PMCPMC8686475
OpenAlexW3207157600

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.