Evidence map›Paper›PMID 26507388›Full record

Trial reportTrials2015

Effects of a prehabilitation program on patients' recovery following spinal stenosis surgery: study protocol for a randomized controlled trial.

Andrée-Anne Marchand, Margaux Suitner, Julie O'Shaughnessy, Claude-Édouard Châtillon, Vincent Cantin, Martin Descarreaux

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

Trial report in Trials, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02258672 (Effects of a Preoperative Rehabilitation Program on the Recovery of Patients Undergoing Surgery for Lumbar Spinal Stenosis), which is not on this map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.3field-weighted citation impact, top 20% 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.

NCT02258672 nacompletednot on this map

Effects of a Preoperative Rehabilitation Program on the Recovery of Patients Undergoing Surgery for Lumbar Spinal Stenosis: a Feasibility Study.

TypeinterventionalSponsorUniversité du Québec à Trois-RivièresRan2014 to 2020Enrolled68ConditionsLumbar Spinal StenosisArmsPrehabilitation program
3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 20 citations in OpenAlex.

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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 2 institutions in 1 country.

Andrée-Anne MarchandUniversité du Québec à Trois-Rivières, Trois-Rivières, Québec, Canada. andree-anne.marchand@uqtr.ca.
Margaux SuitnerUniversité du Québec à Trois-Rivières, Trois-Rivières, Québec, Canada. margaux.suitner@uqtr.ca.
Julie O'ShaughnessyUniversité du Québec à Trois-Rivières, Trois-Rivières, Québec, Canada. julie.o'shaughnessy@uqtr.ca.
Claude-Édouard ChâtillonCentre de Santé et de Services Sociaux de Trois-Rivières, Trois-Rivières, Québec, Canada. claude-edouard.chatillon@mail.mcgill.ca.
Vincent CantinUniversité du Québec à Trois-Rivières, Trois-Rivières, Québec, Canada. vincent.cantin@uqtr.ca.
Martin DescarreauxUniversité du Québec à Trois-Rivières, Trois-Rivières, Québec, Canada. martin.descarreaux@uqtr.ca.
Université du Québec à Trois-Rivières · CACentre intégré universitaire de santé et de services sociaux de la Mauricie-et-du-Centre-du-Québec · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDegenerative lumbar spinal stenosis is a prevalent condition in adults over the age of 65 and often leads to deconditioning. Although the benefits of surgery outweigh those of conservative approaches, physical rehabilitation may be used to improve function and to minimize the risk of persistent dysfunction. This study protocol was designed to establish the feasibility of a full-scale randomized controlled trial and to assess the efficacy of an active preoperative intervention program on the improvement of clinical parameters and functional physical capacity in patients undergoing surgery for lumbar spinal stenosis. METHODS/

designForty patients will be recruited and randomly allocated to one of the 2 treatment arms: 6 weeks supervised preoperative rehabilitation program (experimental group) or hospital standard preoperative management (control group). The intervention group will be trained three times per week, with each session aiming to improve strength, muscular endurance, spinal stabilization and cardiovascular fitness. Intensity and complexity of exercises will be gradually increased throughout the sessions, depending on each participant's individual progress. Primary outcomes are level of low back disability and level of pain. Secondary outcomes include the use of pain medication, quality of life, patient's global impression of change, lumbar extensor muscles endurance, maximum voluntary contraction of lumbar flexor and extensor muscles, maximum voluntary contraction of knee extensors, active lumbar ranges of motion, walking abilities, and cardiovascular capacity. Both the primary and secondary outcomes will be measured at baseline, at the end of the training program (6 weeks after baseline evaluation for control participants), and at 6 weeks, 3 and 6 months postoperatively. DISCUSSION: This study will inform the design of a future large-scale trial. Improvements of physical performances before undergoing lumbar surgery may limit functional limitations occurring after a surgical intervention. Results of this study will provide opportunity to efficiently improve spinal care and advance our knowledge of favorable preoperative strategies to optimize postoperative recovery.

trial registrationUS National Institutes of Health Clinical Trials registry NCT02258672 , 10 February 2014.

Indexed as

Back MusclesBiomechanical PhenomenaClinical ProtocolsDisability EvaluationExercise TherapyFeasibility StudiesHealth StatusHumansLumbar VertebraeMuscle ContractionMuscle StrengthOrthopedic ProceduresPain MeasurementPilot ProjectsPostoperative PainPreoperative Care

Identifiers

PMID26507388
PMCPMC4623294
OpenAlexW2165457254

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.