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NCT Number: NCT02093312

Meals on Wheels, the Effect of a Home Food-delivery Service for Cancer Patients

The overall objective of the study is to investigate the effect of energy- and protein enriched home delivered meals vs. habitual diet in malnourished patients suffering from cancer on various endpoints.

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Key information

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Herlev University Hsopital

Herlev, 2730, Denmark

About this study

Despite the fact that nutritional deterioration has been associated with patients' functional impairment, the effect of individualized nutritional support or counselling to outpatients, focussing on ordinary food, have not yet been thoroughly explored (Ravasco P. et al. 2007). A few studies have investigated the effect of nutritional counselling on quality of life (QoL) in cancer patients after discharge (Ovesen et al. 1993, Persson et al. 2002, Isenring et al. 2004, Ravasco et al. 2005a, Ravasco et al. 2005b). However, there is to our knowledge not conducted any studies examining the effect of home delivered meals on QoL and other endpoints in outpatients suffering from cancer.

The overall objective of the study is to measure the effect of energy- and protein enriched home delivered meals vs. habitual diet in malnourished outpatients diagnosed with lung cancer. The intervention diet will consist of optional protein- and energy-dense main and in-between-meals. There will be 22 different main meals and 13 in-between meals to choose between. The meals are prepared by The Nordic Kitchen of Copenhagen University Hospital Herlev. The offered main meals will consist of a selection of warm dishes taken from the ordinary menu. The in-between meals are a collection of the Delights of Herlev (dishes previously shown to increase dietary intake among in-patients). The food will be delivered to the participants' home 3 times per week, and participants can order one warm dish and ad libitum in-between meals for each day.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Have a nutritional risk score ≥ 3 according to NRS-2002 (Kondrup J. et al. 2003)
  • Be diagnosed with lung cancer
  • Have a life expectancy > 12 weeks
  • Not plan to loose weight or go on a diet
  • Not plan to go on vacation for > 2 weeks during the study period
  • Live at their own home
  • Live ≤ 25 km from the hospital
  • Be able to read, write and understand Danish

Exclusion criteria

  • Receives food from a food-delivery service
  • Have food allergies or intolerance
  • Exclusively receives enteral or parenteral nutrition
  • Suffers from cognitive impairment e.g. dementia
  • Is terminal

Treatment and study plan

Home food-delivery service

Dietary Supplement

A home food-delivery service is offered the intervention group of cancer patients

Primary outcomes

  1. Quality of Life

    Time frame: 6 weeks (change from baseline)

    To assess the Global QoL, a questionnaire from the European Organization for the Research and Treatment of Cancer (EORTC) QLQ-30, version 3, will be used. This is a validated, cancer-specific questionnaire with a total of 30 questions, looking back at the past week. The scoring of QoL is based on 2 specific questions with response options ranging from 1-7 which indicate very bad to very good. A Danish version of the questionnaire will be used.

  2. Quality of Life

    Time frame: 12 weeks (change from baseline)

    To assess the Global QoL, a questionnaire from the European Organization for the Research and Treatment of Cancer (EORTC) QLQ-30, version 3, will be used. This is a validated, cancer-specific questionnaire with a total of 30 questions, looking back at the past week. The scoring of QoL is based on 2 specific questions with response options ranging from 1-7 which indicate very bad to very good. A Danish version of the questionnaire will be used.

Secondary outcomes

  1. Hand grip strength

    Time frame: 6, and 12 weeks (changes from baseline)

    Hand grip strength (in kg) will be measured with a Hydraulic Hand Dynamometer. Participants will be seated with forearms rested on the arms of the chair. They are asked to perform three maximum force trials with their dominant hand and using the second handle position. The test will be repeated within 30 seconds, and the maximum grip score from the three measured values will be used.

  2. 30-second chair-stand test

    Time frame: 6, and 12 weeks (changes from baseline)

    The 30-second-chair-stand test consist of manually counting the number of sit-stand-sit cycles completed during the 30 seconds of the test. A standard chair (with a seat height of 40cm) with or without a backrest but with armrests will be used. Initially, subject will be seated on the chair with their back in an upright position. They will be instructed to rise after the "1, 2, 3, go" command at their own preferred speed with their arms folded across their chest. If the participant is only able to perform the test by using armrest, the test will be recorded as "modified".

  3. Body Weight

    Time frame: 6, and 12 weeks (changes from baseline)

    Body weight will be measured to the nearest 0.1 kg following standard procedures (i.e. without shoes, minimal clothing).

  4. Depression Scale

    Time frame: 6, and 12 weeks (changes from baseline)

    The Center for Epidemiological Studies Depression scale (CES-D) is a short self-report scale designed to measure depressive symptoms (Hann D. et al. 1999). The questionnaire contains 20 items, divided in four domains: Somatic Retarded Activity (7 items), Depressed Affect (5 items), Positive Affect (4 items), and Interpersonal Affect (2 items), and 2 single items that complete the total score. The total score ranges from 0 to 60; a score of ≥16 indicates a depressed symptomatology. The CES-D has been validated in several samples of cancer patients, and it is often administered to inpatients with cancer (Vodermaier A. et al. 2009). A Danish version of the questionnaire will be used.

  5. Total energy- and protein intake per day

    Time frame: 6, and 12 weeks (changes from baseline)

    Dietary intake will be assessed by a dietary interview covering patient's dietary intake over the past week. On basis of the dietary interview the total energy and protein intake per day is estimated. A food database with energy- and protein content of various foods is used for the estimation.

  6. Re-admissions with total length of stay (LOS)

    Time frame: 12 weeks, and 6 months

    Data on re-admissions to the hospital and LOS will be collected from all participants medical charts (hospital medical system OPUS/GS).

  7. Mortality

    Time frame: 12 weeks, and 6 months

    Data on mortality will be collected from all participants' medical charts (hospital medical system OPUS/GS).

  8. WHO Performance status

    Time frame: 6, and 12 weeks

  9. Functional-score

    Time frame: 6 and 12 weeks

    Using EORTC-QLQ-30 version 3 - looking back at the past week. Out of the 30 questions the functional score is based on 15 specific questions with 4 response options indicating either: not at all, a little, some or a lot. Involves questions related to physical-, role-, emotional-, cognitive- and social functioning.

  10. Symptom-score

    Time frame: 6 and 12 weeks (changes from baseline)

    Using EORTC-QLQ-30 version 3 - looking back at the past week. Out of the 30 questions the symptom score is based on 13 specific questions with 4 response options indicating either: not at all, a little, some or a lot.

Other outcomes

  1. Compliance

    Time frame: 1, 6, and 12 weeks

    All patients in the intervention group are requested to daily fulfil a compliance sheet during the whole 12-week period, where the intake of intervention dishes will be recorded. Project staff will review the completed sheets together with the study participant at mid-way (week 6) and at the final 12-week visit in order to minimize possible uncertainties. Moreover, eventual side-effects and reasons for non-compliance will be recorded.

  2. Evaluation

    Time frame: 12 weeks

    All the intervention participants will receive an evaluation form in order to assess the acceptability of the offered meals, the food-delivery service, and a possible price they would give for this particular food-delivery service.

  3. Effect of social status on total energy- and protein intake

    Time frame: Baseline

    Definition of social status: if the participant is living alone or not

  4. Correlation between compliance (intervention group) and Quality of life

    Time frame: 12 weeks

  5. Correlation between total energy- and protein intake (all participants) and Quality of life

    Time frame: 12 weeks

  6. Correlation between compliance (intervention group) and Body weight

    Time frame: 12 weeks

  7. Correlation between compliance (intervention group) and Hand grib strength

    Time frame: 12 weeks

  8. Correlation between compliance (intervention group) and 30-second chair-stand test

    Time frame: 12 weeks

  9. Correlation between compliance (intervention group) and Depression score

    Time frame: 12 weeks

  10. Correlation between compliance (intervention group) and Total energy- and protein intake

    Time frame: 12 weeks

  11. Correlation between compliance (intervention group) and WHO performance status

    Time frame: 12 weeks

  12. Correlation between total energy- and protein intake (all participants) and Hand grip strength

    Time frame: 12 weeks

  13. Correlation between total energy- and protein intake (all participants) and Body weight

    Time frame: 12 weeks

  14. Correlation between total energy- and protein intake (all participants) and 30 second chair-stand test

    Time frame: 12 weeks

  15. Correlation between total energy- and protein intake (all participants) and Depression scale

    Time frame: 12 weeks

  16. Correlation between total energy- and protein intake (all participants) and WHO performance status

    Time frame: 12 weeks

Sponsors and collaborators

Lead sponsor

Copenhagen University Hospital at Herlev

Other

Registry information

Official study title

Meals on Wheels, a Randomized Controlled Study on the Effect of a Home Food-delivery Service for Cancer Patients

Acronym: RUMLE

Important dates

Study start
2014
Primary completion
2014
Study completion
2015
First posted
Mar 21, 2014
Registry last updated
Dec 21, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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