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Virtual Group Prehabilitation Education (Surgery School) Feasibility Trial (GoPREPARE)

U

University Hospital Southampton NHS Foundation Trust

Status

Enrolling

Conditions

Elective Surgery
Patient Education
Cancer Surgery
Prehabilitation

Treatments

Other: GoPREPARE

Study type

Interventional

Funder types

Other

Identifiers

NCT07278622
RHM CRI0467

Details and patient eligibility

About

One in four patients requiring planned major surgery have complications. Prehabilitation; which involves increasing physical activity, improving nutrition and supporting emotional well-being prior to surgery can reduce these complications and improve recovery. Group preoperative prehabilitation classes (surgery schools) are advocated by the Centre for Perioperative Care and are standard care in many hospitals, despite a lack of evidence for their effectiveness in improving patient outcomes. In phase 1 an 2 of this research investigators used patient experiences and co-participatory methods to optimise an existing intervention to make it as acceptable and as engaging as possible. The resulting education package is called 'GoPREPARE'

Investigators now intend to test the practicalities of trialing GoPREPARE on preoperative patients with cancer. 24 patients awaiting surgery will be recruited from University Hospital Plymouth and randomly allocated equally to: Group - GoPREPARE and Group 2- standard care. Participants will complete lifestyle questionnaires before during and after their hospital stay. To evaluate the experience, ~8 participants will be interviewed. 5 clinical staff involved in the trial will also take part in a focus group. The information collected will be analysed to assess if it is feasible to conduct a larger trial.

Full description

See uploaded protocol

Enrollment

24 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adults undergoing elective surgery for any body cavity cancer with curative intent.
  • Adults with more than 3 weeks before planned surgery
  • Adults without previous experience of prehabilitation.

Exclusion criteria

  • Children
  • Adults who lack mental capacity.
  • Adults who do not understand spoken English.
  • Previous experience of prehabilitation.
  • Previous surgery for cancer
  • Pregnancy

Trial design

Primary purpose

Prevention

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

24 participants in 2 patient groups

GoPREPARE Education Intervention
Experimental group
Description:
A 1.5 live education webinar delivered to groups of patients and their carers before surgery. Delivered by health care professionals.
Treatment:
Other: GoPREPARE
Standard Care
No Intervention group
Description:
Patients will be given a standard prehabilitation leaflet

Trial contacts and locations

1

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Central trial contact

Sharon Davies-Dear; Imogen C Fecher-Jones, MSc

Data sourced from clinicaltrials.gov

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