Welcome
Support Centre
02 September 2010 
Current Controlled Trials - Clinical Trials
Trial registration
Unique identification scheme
International databases
home  |   my details  |   ISRCTN Register  |   mRCT  |   links  |   information  |   news
Introduction
English introduction Introduction en français Deutsche einleitung
Introducción española Introduzione in italiano
 
Find trials
active registers
mental health register
archived registers
all registers
tips on searching
 
 
Information
about mRCT
mRCT FAQs

DISCLAIMER
The site should not be used to diagnose or treat a health problem. Please consult your doctor.
Terms & conditions

DUPLICATION
Your search result may contain a number of different records for the same trial. This occurs when the same trial is listed in more than one register.

[ ...Back to search results ] [ Print-friendly version ]
Effect of early mobilisation on respiratory complications following abdominal surgery
Source of recordUK Trials
ISRCTNISRCTN28048472
Date ISRCTN assigned11/04/2008
Local reference number(s)sm110208/00
Public titleEffect of early mobilisation on respiratory complications following abdominal surgery
Scientific titleEffect of post-operative early mobilisation on pulmonary complications and hospital stay: a randomised trial
AcronymN/A
Disease/condition/study domainElective upper and lower gastrointestinal (GI) surgery
Study hypothesisEarly mobilisation is used by many centres around the country, with physiotherapists hypothesising that movement will encourage deeper breaths due to increasing oxygen demand, improve muscle strength and patient confidence, reduce post-operative pulmonary complications (PPCs) and ultimately reduce length of stay. The aim of this study is to establish whether goal oriented early post-operative mobilisation would reduce post-operative pulmonary complications and reduce hospital length of stay in patients who have had elective abdominal surgery.
Design/methodologyParallel-group, single blinded, single centre, randomised clinical trial
Research ethics reviewPending as of 12/02/2008: Ethics committee requires investigators to have registered with ISRCTN before considering their applications.
Countries of trialUnited Kingdom
Participants - inclusion criteria1. Elective patients
2 Abdominal surgery
3. Booked in High Dependency Unit (HDU)
4. Ability to give written informed consent prior to study participation
5 Male or female patients over 18 years old
6. Ability to communicate with the study personnel and to comply with the study requirements
7. Ability to mobilise (freely or with walking aid)
8. American Society of Anaesthesiologists (ASA) grade 1 - 3 inclusive
Participants - exclusion criteria1. Inability to communicate with the study personnel and to comply with the study requirements (mobility)
2. Unable to give consent
3. Under 18 years of age
4. Patients admitted to Intensive Care Unit (ICU) prior to HDU
5. Patients with impaired mobility (bed bound or wheel chair bound)
6. ASA grade 4 or above
Patient information materialNot available in web format, please use the contact details below to request a patient information sheet
Anticipated start date01/05/2008
Anticipated end date01/05/2009
Status of trialOngoing
Target number of participants200 (100 in each group - upper and lower GI surgery)
Interventions1. Control group: routine post-operative physiotherapy
2. Intervention group: routine post-operative physiotherapy and goal directed mobilisation

Patients will be encouraged to achieve progressive mobility goals as shown:
1. Up to sit out of bed
2. Mobilise 5 m assisted
3. Mobilise 20 m assisted
4. Mobilise 40 m independently

Each patient will be treated once each day, unless clinical need indicates further respiratory intervention. All patients will be reviewed for a minimum of 7 days post operatively, and until they have returned to their previous level of function.
Primary outcome measure(s)1. Post-operative pulmonary complications: both the number of patients with these complication and the severity will be taken into account
2. Pulmonary function tests: the forced expiratory volume in one second (FEV1) and forced vital capacity (FVC) will be collected pre-operatively and post-operatively on days 3, 5 and prior to hospital discharge
Secondary outcome measure(s)1. HDU stay
2. Hospital stay
Sources of fundingChief Scientist Office (CSO) (UK) - research grant pending
Sponsor nameUniversity of Dundee (UK)
Sponsor detailsc/o Mr S Shimi
Ninewells Hospital
Ninewells Avenue
Dundee
United Kingdom
DD1 9SY
Sponsor websitehttp://www.dundee.ac.uk/
Contact nameMr Sami Shimi
Contact detailsDundee University and Medical School
Ninewells Hospital
Dundee
United Kingdom
DD1 9SY
More informationFor more up-to-date information please go to the ISRCTN link below.
Link to record in ISRCTN RegisterISRCTN28048472
Date last extracted from ISRCTN register17/04/2008
Submit your trial protocol
Submit to Trials journal
Follow us on Twitter
© 2010 Current Controlled Trials Ltd. Part of Springer Science+Business Media. | terms & conditions | privacy statement


BioMed Central