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Individualised nutritional counselling for patients who have undergone major upper gastrointestinal surgery - a randomised controlled trial

A randomised controlled trial assessing weight change in individualised nutritional counselling for patients who have undergone major upper gastrointestinal surgery

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12609000219280
Enrollment
30
Registered
2009-04-30
Start date
2009-04-01
Completion date
2011-11-30
Last updated
2020-01-13

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

Conditions

None listed

Brief summary

Current practice is that once patients are discharged from hospital after surgery they do not have dietetic follow up. The aim of this study is to investigate whether individualised nutrition counselling improves nutritional status and quality of life in the 6 months post-discharge.

Interventions

All patients will recieve a one-on-one 30 minute nutrition counselling session with a Dietitian on the ward prior to discharge to discuss eating after surgery. Basic information is covered such as small frequent meals and high energy/protein food choices. This is current practice. Then patients are randomised into a control group or intervention. The intevention group are contacted by the Dietitian by phone every 2 weeks for 6 months and face to face at 1 and 3 months. This nutrition couselling

All patients will recieve a one-on-one 30 minute nutrition counselling session with a Dietitian on the ward prior to discharge to discuss eating after surgery. Basic information is covered such as small frequent meals and high energy/protein food choices. This is current practice. Then patients are randomised into a control group or intervention. The intevention group are contacted by the Dietitian by phone every 2 weeks for 6 months and face to face at 1 and 3 months. This nutrition couselling will include assessing intake, weight and symptoms, and giving relevant nutrition advice based on this.

Sponsors

Royal Prince Alfred Hospital
Lead SponsorHospital

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Educational / counselling / training
Masking
Blinded (masking used)

Eligibility

Sex/Gender
All
Age
18 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

All patients undergoing Ivor-lewis Oesphagectomy, Partial or Total Gastrectomy, or Whipples surgery for non-neoplasm or curative neoplasm reasons.

Exclusion criteria

Known metastatic disease Rural patient not to be followed up by Royal Prince Alfred Hospital (RPAH) surgeons

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026