The Impact of Preoperative FoodforCare at Home

NCT ID: NCT03488511

Last Updated: 2020-02-19

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

126 participants

Study Classification

INTERVENTIONAL

Study Start Date

2018-03-05

Study Completion Date

2019-09-01

Brief Summary

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Preoperative nutritional state is closely related to perioperative morbidity and complications. This study aims to determine the effect of a protein-rich meal service in the preoperative setting compared to usual care.

Detailed Description

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Each year, approximately 1.4 million patients in the Netherlands are operated. Adequate nutritional intake, mainly protein intake, before surgery is important to improve preoperative muscle strength and functional capacity. However, up to 40% of patients admitted to the hospital suffer from malnutrition and this further deepened during hospitalization, which is an independent risk factor for peri-operative morbidity and severe complications, ranging from increased muscle loss, to higher infection rates, delayed wound healing and subsequently a prolonged hospital stay. An adequate food service is one strategy to improve protein intake and thereby the nutritional status. Extension of the study period to the out-of-hospital setting is recommended to explore the effects of long-term exposure to this concept on nutritional, functional and clinical outcomes. Therefore, the investigators aim to evaluate whether home delivered protein-rich meals, as part of FoodforCare meal service, in the preoperative setting improves protein intake in patients undergoing surgery, compared to usual care. The second aim is to investigate the effects on functional and clinical outcomes.

Conditions

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Surgery

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

SUPPORTIVE_CARE

Blinding Strategy

NONE

Study Groups

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Intervention group

The intervention group will receive meals from FoodforCare at Home. The FoodforCare at Home concept consists of six small protein and energy enriched meals and snacks that will be delivered twice a week. After an individual intake, the composition of the dishes will be tailored to the needs of the patient in terms of composition, diet, taste, flavor and portion size. Besides the meals, patients in the intervention group will also receive an information leaflet about the importance of protein during treatment and how to reach their protein requirements.

Group Type EXPERIMENTAL

FoodforCare at home

Intervention Type OTHER

Six small protein rich meals that will be delivered twice a week for 3 weeks.

Control group

The control group will continue their usual diet for 3 weeks and have no restrictions to their diet.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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FoodforCare at home

Six small protein rich meals that will be delivered twice a week for 3 weeks.

Intervention Type OTHER

Eligibility Criteria

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Inclusion Criteria

* 18 years or older
* surgical patients
* living within a 40 km radius around Nijmegen/Veghel
* inclusion at least 4 weeks before surgery
* surgery: Urology, Orthopedics, Gynaecology, General Surgery
* oral intake

Exclusion Criteria

* renal insufficiency (MDRD-GFR (glomerular filtration rate) \< 60ml/min and/or proteinuria)\*
* food allergy
* planned vacation during intervention period

* proteinuria is defined in case of a protein creatinine ratio \> 0.5g/10mmol or an albuminuria \> 300mg/day.
Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Radboud University Medical Center

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Manon van den Berg, PhD

Role: STUDY_CHAIR

Radboud University Medical Center

Locations

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Radboudumc

Nijmegen, Gelderland, Netherlands

Site Status

Maasziekenhuis Pantein

Beugen, North Brabant, Netherlands

Site Status

Countries

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Netherlands

Provided Documents

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Document Type: Study Protocol and Statistical Analysis Plan

View Document

Other Identifiers

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2016-3043

Identifier Type: -

Identifier Source: org_study_id

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