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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02667795
Other study ID # SNE 2447
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date October 2016
Est. completion date November 21, 2019

Study information

Verified date October 2020
Source York Teaching Hospitals NHS Foundation Trust
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

It is generally accepted that physically fit patients cope much better with the stress of surgery and recover faster. Consequently several research studies have tried to increase people's level of fitness before they have surgery. These previous research studies have usually required patients to carry out intense, structured exercise programmes that involve going to a gym. However such programmes are not 'user friendly' especially if people are not used to taking a lot of exercise. In this pilot study we want to test the feasibility of a home based programme that tries to increase patients' level of fitness by gradually increasing the number of steps they walk every day.


Description:

Participants will be randomised into one of two groups. One group of participants will be asked to increase their level of activity by gradually walking further (the exercise group) and the other group will carry on with their usual level of activity (the usual activity group) . Assessments People in both groups will have an assessment on 3 occasions: when they join the study, just before surgery and 3 months after surgery. This assessment involves: Walking for 6 minutes up and down a corridor to see how far they can walk. Asking them for some information about their medical history Completing three questionnaires about how they are feeling and their quality of life. People who are randomised to the exercise group will be advised about how many steps to take based on how they did in the initial walking assessment. The number of days or weeks they will be asked to take a daily walk will depend on how much time there is between them joining the study and the date of their surgery. We think this will be about 2 weeks.


Recruitment information / eligibility

Status Completed
Enrollment 40
Est. completion date November 21, 2019
Est. primary completion date November 21, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Aged 18 years or older - Requiring elective resectional bowel surgery - Gives consent to participate in the study Exclusion Criteria: - Younger than 18 years of age. - A history of unstable angina/unstable coronary artery disease or a heart attack in the previous month. - Any heart related disease including but not limited to aortic stenosis, pericarditis or any thromboembolic disease. - Severe Infections and fever. - Uncontrolled metabolic diseases. - Resting heart rate of more than 120 BPM. - Systolic blood pressure of more than 180 mm Hg or diastolic blood pressure of more than 110 mm Hg. - Recent cerebrovascular accident. - Pregnancy - Pre-existing severe physical disability. - Unwilling to allow their GP to be informed of their participation in the study. - Not able or unwilling to consent to take part in the study

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Monitored walking based exercise
Monitored walking based exercise

Locations

Country Name City State
United Kingdom Scarborough General Hospital Scarborough Yorkshire

Sponsors (1)

Lead Sponsor Collaborator
York Teaching Hospitals NHS Foundation Trust

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in fitness as assessed by Six Minute Walk Test Fitness assessment Will be done at recruitment, prior to surgery and 3 months post operatively
Secondary The EQ-5D Quality of life assessment Will be done at recruitment, prior to surgery and 3 months post operatively
Secondary EORTC QLC-C30 Quality of life assessment Will be done at recruitment, prior to surgery and 3 months post operatively
See also
  Status Clinical Trial Phase
Withdrawn NCT00456703 - Restricted Fluid Regimen in Open Abdominal Bowel Surgery N/A