Evidence map›Paper›PMID 28270180›Full record

Trial reportTrials2017

Randomized trial of acupressure to improve patient satisfaction and quality of recovery in hospitalized patients: study protocol for a randomized controlled trial.

Eric Noll, Shivam Shodhan, Maria Cecilia Madariaga, Christopher R Page, Diane Santangelo, Xiaojun Guo, Ehab Al Bizri, Aurora D Pryor, Jamie Romeiser, Elliott Bennett-Guerrero

Registry-linked trialOpen access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Trials, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02762435 (Randomized Controlled Trial of Acupressure to Improve Patient Satisfaction and Quality of Recovery in Hospitalized Patients), which is not on this map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
2.7field-weighted citation impact, top 11% 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.

NCT02762435 nacompletednot on this map

Randomized Controlled Trial of Acupressure to Improve Patient Satisfaction and Quality of Recovery in Hospitalized Patients

TypeinterventionalSponsorStony Brook UniversityRan2016 to 2017Enrolled200ConditionsAcupressureArmssham, control, acupressure
3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 16 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Article
  5. 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

10 authors at 1 institution in 1 country.

Eric NollDepartment of Anesthesiology Stony Brook Medicine, Stony Brook, NY, USA. eric.noll@chru-strasbourg.fr.
Shivam ShodhanDepartment of Anesthesiology Stony Brook Medicine, Stony Brook, NY, USA.
Maria Cecilia MadariagaDepartment of Anesthesiology Stony Brook Medicine, Stony Brook, NY, USA.
Christopher R PageDepartment of Anesthesiology Stony Brook Medicine, Stony Brook, NY, USA.
Diane SantangeloDepartment of Anesthesiology Stony Brook Medicine, Stony Brook, NY, USA.
Xiaojun GuoDepartment of Anesthesiology Stony Brook Medicine, Stony Brook, NY, USA.
Ehab Al BizriDepartment of Anesthesiology Stony Brook Medicine, Stony Brook, NY, USA.
Aurora D PryorDepartment of Surgery Stony Brook Medicine, Stony Brook, NY, USA.
Jamie RomeiserDepartment of Anesthesiology Stony Brook Medicine, Stony Brook, NY, USA.
Elliott Bennett-GuerreroDepartment of Anesthesiology Stony Brook Medicine, Stony Brook, NY, USA.
Stony Brook Medicine · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAcupressure therapy may be potentially beneficial in improving postoperative symptoms like postoperative nausea and vomiting (PONV), pain and sleep disorder and improving postoperative quality of recovery. The primary aim of this study is to investigate the efficacy of acupressure therapy on postoperative patient satisfaction and quality of recovery in hospitalized patients after surgical treatment. METHODS/

designThis three-group, parallel, superiority, blinded, randomized controlled trial will test the hypothesis that a combination of PC6, LI4 and HT7 acupressure is superior to sham or no intervention for improving postoperative quality of recovery in hospitalized patients. A minimum of 150 patients will be randomly allocated to one of the three experimental groups: control (no visit), light touch (sham acupressure) or active acupressure therapy in a 1:1:1 ratio. Interventions will be performed three times a day for 2 days. Patient satisfaction, quality of recovery, PONV and pain will be measured during the 3 days following randomization. The study protocol was approved by the Stony Brook University Institutional Review Board on 21 March 2016. Written informed consent will be recorded from every consented patient. DISCUSSION: This study has the potential to improve the recovery of hospitalized patients by adding knowledge on the efficacy of acupressure therapy in this setting. A multipoint acupressure protocol will be compared to both a no intervention group and a light touch group, providing insight into different aspects of the placebo effect.

trial registrationClinicalTrial.gov, NCT02762435 . Registered on 14 April 2016.

Indexed as

HospitalizationPatient SatisfactionAcupressureClinical ProtocolsHumansNew YorkPain MeasurementPostoperative Nausea and VomitingPostoperative PainRecovery of FunctionResearch DesignSurgical Procedures, OperativeSurveys and QuestionnairesTime FactorsTreatment OutcomeAcupressure therapyPatient satisfactionQuality of recovery

Identifiers

PMID28270180
PMCPMC5341349
OpenAlexW2594034383

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.