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Preoperative walking exercise to improve prognosis in patients with supratentorial brain tumours after craniotomy: protocol for a randomised controlled trial.

BMJ open
January 1, 1970
Chunrun Qu et al. (6 authors)
Journal ArticleClinical Trial ProtocolResearch Support, Non-U.S. Gov'tHuman StudyClinical
Study Details

Study Goal

The researchers aimed to determine whether preoperative walking exercise could reduce cardiopulmonary complications and preserve cognitive function in brain tumor patients undergoing craniotomy.

Results Summary

The study anticipates that short-term preoperative walking (10,000-15,000 steps/day) will reduce surgery-related complications, protect cognitive function, aid recovery, and lower treatment costs, though final results are pending.

Population

Adults aged 18-65 with supratentorial brain tumors, preoperative waiting time >3-4 weeks, and no cognitive impairment.

Effective Dosage

10,000-15,000 steps per day

Duration

3-4 weeks

Interactions

None mentioned

Extracted Claims (6)
InterventionDirectionEndpointPopulationDosageImpactClaim #
walking exercise prior to craniotomy
decrease
cardiopulmonary complications
brain tumour patients
-
reduce the incidence
#1
walking exercise prior to craniotomy
no change
cognitive function
brain tumour patients
-
preserve
#2
walking exercise prior to craniotomy
decrease
surgery-related complications
brain tumour patients
-
reduce the incidence
#3
walking exercise prior to craniotomy
no change
cognitive function
brain tumour patients
-
protect
#4
walking exercise prior to craniotomy
increase
postoperative recovery
brain tumour patients
-
aid
#5
walking exercise prior to craniotomy
decrease
financial cost of treatment
brain tumour patients
-
reduce
#6
Abstract

INTRODUCTION: Cardiopulmonary complications and cognitive impairment following craniotomy have a significantly impact on the general health of individuals with brain tumours. Observational research indicates that engaging in walking is linked to better prognosis in patient after surgery. This trial aims to explore whether walking exercise prior to craniotomy in brain tumour patients can reduce the incidence of cardiopulmonary complications and preserve patients' cognitive function. METHODS AND ANALYSIS: In this randomised controlled trial, 160 participants with supratentorial brain tumours aged 18-65 years, with a preoperative waiting time of more than 3-4 weeks and without conditions that would interfere with the trial such as cognitive impairment, will be randomly assigned in a ratio of 1:1 to either receive traditional treatment or additional combined with a period of 3-4 weeks of walking exercise of 10 000-15 000 steps per day. Wearable pedometer devices will be used to record step counts. The researchers will evaluate participants at enrolment, baseline, 14 days preoperatively, 3 days prior to surgery and 1 week after surgery or discharge (select which occurs first). The primary outcomes include the incidence of postoperative cardiopulmonary complications and changes in cognitive function (gauged by the Montreal Cognitive Assessment test). Secondary outcomes include the average length of hospital stay, postoperative pain, participant contentment, healthcare-associated costs and incidence of other postoperative surgery-related complications. We anticipate that short-term preoperative walking exercises will reduce the incidence of surgery-related complications in the short term after craniotomy, protect patients' cognitive function, aid patients' postoperative recovery and reduce the financial cost of treatment. ETHICS AND DISSEMINATION: The study protocol has been approved by Ethics Committee of Xiangya Hospital of Central South University (approval number: 202305117). The findings of the research will be shared via publications that have been reviewed by experts in the field and through presentations at conferences. TRIAL REGISTRATION NUMBER: NCT05930288.

Medical Subject Headings (MeSH)
HumansCraniotomyWalkingAdultMiddle AgedSupratentorial NeoplasmsFemaleMaleAgedPreoperative ExercisePrognosisRandomized Controlled Trials as TopicYoung AdultPostoperative ComplicationsAdolescentCognition
Study Links
Quality Scores
SafetyNot Assessed
Efficacy85/10
Quality90/10
Research Impact Scores
APT Score0.05
Weight Score1.44
Normalized Score0.72
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