Evidence map›Paper›PMID 31286999›Full record

ArticleTrials2019

Investigating the effect of Eye Movement Desensitization and Reprocessing on pain intensity in patients with primary dysmenorrhea: a protocol for a randomized controlled trial.

Sahar Valedi, Zainab Alimoradi, Mohammad MoradiBaglooei, Amir H Pakpour, Mehdi Ranjbaran, Venus Chegini

Open access · goldAbstract readClinical Trial Protocol
In one paragraph

Article in Trials, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.9field-weighted citation impact, top 23% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

  1. Trial
  2. Trial
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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

6 authors at 3 institutions in 2 countries.

Sahar ValediStudents Research Committee, School of Nursing & Midwifery, Qazvin University of Medical Sciences, Bahonar blv, Qazvin, 34197-59811, Iran.
Zainab AlimoradiSocial Determinants of Health Research Center, Qazvin University of Medical Sciences, Bahonar blv., Qazvin, 34197-59811, Iran. z.alimoradi@qums.ac.ir.ORCID http://orcid.org/0000-0001-5327-2411
Mohammad MoradiBaglooeiSchool of Nursing & Midwifery, Qazvin University of Medical Sciences, Bahonar blv, Qazvin, 34197-59811, Iran.
Amir H PakpourSocial Determinants of Health Research Center, Qazvin University of Medical Sciences, Bahonar blv., Qazvin, 34197-59811, Iran.
Mehdi RanjbaranDepartment of Epidemiology, School of Public Health, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Venus CheginiObstetrics and Gynecology Department, School of Medicine, Qazvin University of Medical Sciences, Qazvin, Iran.
Qazvin University of Medical Sciences · IRIranshahr University · IRShahid Beheshti University of Medical Sciences · IR

Funding

Qazvin University of Medical Sciences 138/D
6 · The paper itself

Abstract

backgroundUnpleasant experience with the previous menstruation can increase the sensitivity to pain which may lead to moderate to severe pain in patients with dysmenorrhea. Eye movement desensitization and reprocessing (EMDR) is a psychological method to alleviate the distress from unpleasant memories and related events and can be used for other conditions such as anxiety, depression, and chronic pain. This protocol was designed to investigate the effect of EMDR therapy on pain intensity in patients with dysmenorrhea. METHODS/

designA randomized clinical trial was designed in compliance with the Consolidated Standards of Reporting Trials (CONSORT). Female students who have moderate to severe primary dysmenorrhea (based on a visual analogue scale [VAS] score of at least 4 for two consecutive months) and who live in dormitories at Qazvin University of Medical Sciences in Qazvin, Iran will be invited to participate in the study. The total sample size will be 88 girls, who will be randomly assigned to intervention (N = 44) and control (N = 44) groups. EMDR therapy will be performed for the intervention group, while the control group can use sedative or other pain relife methods as their routin... There will be six treatment sessions, which will be held twice a week. The duration of each session is 30-90 min, according to the convenience of each participant. The data will be collected using the demographic characteristics questionnaire, the VAS, the Subjective Units of Anxiety or Distress Scale (SUD), and the Validity of Cognition Scale (VOC). The data on pain intensity due to primary dysmenorrhea in both groups will be collected at 1 and 2 months before the intervention (to identify eligible participants) and 1 and 2 months after the intervention (follow-ups). Data will be analyzed by using SPSS version 25 software and analysis of variance (ANOVA) with repeated measures with appropriate post hoc tests. A P value of less than 0.05 will be considered significant. DISCUSSION: The results are expected to provide the information on the efficacy of EMDR therapy to manage moderate to severe pain in patients with primary dysmenorrhea. ETHICS AND DISSEMINATION: The research proposal is approved by the human ethics committee of Qazvin University of Medical Sciences (IR.QUMS.REC.1397.100). The results of this trial will be submitted for publication in a peer-reviewed research journal.

trial registrationIRCT20180823040851N1 . Registered on 6, October 2018.

Indexed as

Eye Movement Desensitization ReprocessingPain PerceptionPain ThresholdAdolescentAdultDysmenorrheaFemaleHumansIranPain MeasurementRandomized Controlled Trials as TopicTime FactorsTreatment OutcomeYoung AdultEMDR therapyPain managementPrimary dysmenorrhea

Identifiers

PMID31286999
PMCPMC6615253
OpenAlexW2961360378

What OpenQuestion holds

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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.