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Improving the Quality of Life of Cancer Patients Through a Perioperative and Coordinated Nutrition and Physical Care Program.

Improving the Quality of Life of Cancer Patients Through a Perioperative and Coordinated Nutrition and Physical Care Program.

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03670199
Acronym
PENDICOQ
Enrollment
200
Registered
2018-09-13
Start date
2019-01-29
Completion date
2024-04-28
Last updated
2021-09-13

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

Conditions

Digestive Cancer, Undernourished

Brief summary

Hospitalization, for cancer patients, exposes to a risk of undernutrition which has the effect of significantly increasing infections, pressure ulcers, muscle wasting, loss of autonomy, impaired function and delayed healing. All of these factors contribute to increase the length of stay in hospital, thus lengthening the spiral of undernutrition, which has serious consequences for the patient welbeing, health establishments and public health. Undernutrition has been the subject of many studies over the last twenty years, that outline that an adequate nutritional management exerts a direct effect on the reduction of comorbidities and duration of hospitalization. However, there are periods, in the preoperative course of care, where nutritional and phisical care are not realized in the current clinical practice whereas they could be done, for example, between the diagnosis and the consultation of anesthesia, between the anesthesia consultation and the surgical procedure and the end of hospitalization of the patient. Current management is usually limited to the period of hospitalization which tends to be reduced. This situation is reinforced by the absence of relays at home, dietary consultations being not reimbursed by French health insurance. Moreover, a preliminary survey, conducted in 2012 during the pre-operative outpatient anesthesia consultation, shows that 26% of patients are already clinically malnourished, with 16.5 % of them who have lost more than 10% of their weight.

Detailed description

Then, the investigators hypothesize that the combination of perioperative nutrition and mobilization program coordinated andrealized by dieticians and physiotherapists, with the Nutrimus follow-up booklet, would improve the post-operative evolution of patients and reduce their postoperative comorbidities. This management, initiated at the consultation of anesthesia, would include an accurate nutritional diagnosis, nutritional and physical support therapy to improve their nutritional and muscular status.

Interventions

OTHERDietary advice

Nutritional status assessment Explanation of standard nutritional advices with an written explanation sheet

OTHERPhysiotherapist intervention

Respiratory capacity Functional capacity

OTHERDietary intervention

Nutritional status assessment Presentation of the Nutrimus booklet by the coordinating dietitian Establishment or adaptation of a nutritional support (prescription of nutritional supplements if necessary). Delivery and explanation of the preoperative nutritional counseling support

OTHERIntensify physiotherapist intervention

Respiratory capacity Functional capacity Tips adapted for physical activity and strengthening or maintenance of muscle mass Presentation of respiratory physiotherapy exercises to prevent postoperative bronchial congestion Nutrition and physical mobilization tips with the Nutrimus booklet

Sponsors

University Hospital, Strasbourg, France
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patient ≥ 18 years old * Patient with Karnofsky index superior or equal to 60%. * Patient with cancer of the following digestive tract: peritoneal carcinoma, sarcoma, pancreas, rectum, esophagus, stomach diagnosed or under diagnosis * Patient admitted for a scheduled surgery at least 10 days after a preoperative consultation * Patient affiliated to a social health insurance scheme * Patient having dated and signed an informed consent * Patient having been informed of the results of the prior medical examination

Exclusion criteria

* Inhospital patients * Patient admitted in emergency * Impossibility of giving the patient information (alteration of patient's cognitive function) * Illiteracy or dyscalculia * Patients protected (guardianship, curatorship, safeguard of justice) * Pregnancy, breastfeeding * Subject in exclusion period (determined by a previous or ongoing study), * Patient included in another ongoing clinical trial * Patient with neuro-endocrine cancer * Patient reoperated for the same pathology

Design outcomes

Primary

MeasureTime frameDescription
Variation of the Medical Outcome Study Short Form 36 scoreChange in score at 30 days before surgery and 1 Day before hospital dischargeUse of a scale for quality of life

Secondary

MeasureTime frameDescription
Satisfaction score of the Nutrimus tool6 months postoperativeUse of a questionnaire
Ease of use of the Nutrimus tool6 months postoperativeUse of a questionnaire
Measurement of the Medical Outcome Study Short Form 36 scoreChange in score at 1 day before surgery, 1 day before the end of hospitalization, 1 Month, 3 Months and 6 Months post hospitalizationUse of a scale for quality of life
Sarcopenia index measurement30 days before surgeryMeasure from routine preoperative Computerized Tomography scan
Evaluation of respiratory and functional capacitiesChange in measures at 30 days to 10 days, 1 day before surgery, 1 day before the end of hospitalization, 1 Month, 3 Months and 6 Months post hospitalization
Pain assessmentChange in score at 30 days to 10 days, 1 day before surgery, 1 day before the end of hospitalization, 1 Month, 3 Months and 6 Months post hospitalizationUse of a visual analogue scale Measure of score from 0 to 10
Length hospitalizationDuration (in days) of patient's hospitalizationLength (in days) between hospital admission and discharge
Evaluation of nutritional parametersChange in values measures at 30 days to 10 days, 1 day before surgery, 1 day before the end of hospitalization, 1 Month, 3 Months and 6 Months post hospitalizationUse of a notebook

Countries

France

Contacts

Primary ContactDRCI Strasbourg
dpidrci@chru-strasbourg.fr0388117438

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026