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Supportive exercise programmes for accelerating recovery after major abdominal cancer surgery

SupPoRtive Exercise Programmes for Accelerating REcovery after major ABdominal Cancer surgery (PREPARE-ABC) – A multicentre, 3 arm, parallel randomised controlled trial of standard care alone versus standard care plus supervised hospital based exercise and standard care plus supported home-based exercise pre and post hospital discharge in cancer patients awaiting curative colorectal cancer surgery

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN82233115
Enrollment
1146
Registered
2016-07-07
Start date
2016-11-01
Completion date
Unknown
Last updated
2025-09-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Colorectal cancer Cancer Malignant neoplasms of digestive organs

Interventions

Current interventions as of 19/08/2019: Control arm: Treatment as Usual (TAU) comprising the patient information leaflet and study follow-up visits only. No other information relating to peri-operativ

Sponsors

Norfolk and Norwich University Hospitals NHS Foundation Trust
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Male and female participants = 18 years old 2. Awaiting a curative elective colorectal resection for cancer 3. American Society of Anaesthesiologists physical status I-III (ASA, 2014) 4. Able and willing to provide informed consent 5. Understand verbal and written instructions in English 6. Patients who are already participating (or have participated) in other trials may be eligible, but this must be agreed in advance by the relevant trial teams

Exclusion criteria

Exclusion criteria: 1. Contra-indications to exercise (e.g. lower limb amputation without prosthesis, orthopaedic disorder exacerbated by exercise, chronic lung disease causing desaturation with exercise or shortness of breath at rest, severe psychiatric health problems) 2. Cardiovascular contraindications (e.g. unstable angina, acute left ventricular failure, uncontrolled cardiac arrhythmias, uncontrolled hypertension, cardiac event in the previous 6 weeks, cerebral vascular disease resulting in transient ischaemic attacks) 3. Participation in other treatment trials, where this has not been agreed in advance with both trial teams

Design outcomes

Primary

MeasureTime frame
Health-related quality of life is measured using the Study Short-Form Health Questionnaire (SF-36) at baseline and 12 months post-randomisation.

Secondary

MeasureTime frame
1. Post-operative morbidity is measured 30 days post-surgery 2. Cardiopulmonary fitness 3. Grip strength 4. Length of hospital stay is recorded at discharge following operation 5. Fitness for discharge is recorded at discharge following operation 6. Re-admission rate is determined 90 days post-surgery 7. Post-operative mortality is measured 90 days post-surgery 8. Physical activity behaviour is measured 6 and 12 months 9. Psychological health status is measured 6 and 12 months

Countries

England, Scotland, United Kingdom

Contacts

Public ContactBeauty Mutandari
B.Mutandari@uea.ac.uk+44 (0)1603 591263

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026