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Spots Global Cancer Trial Database for App-based Recording and Optimization of the Nutritional Status in Patients With Head and Neck Tumors During and After Radio(Chemo)Therapy

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Trial Identification

Brief Title: App-based Recording and Optimization of the Nutritional Status in Patients With Head and Neck Tumors During and After Radio(Chemo)Therapy

Official Title: App-based Recording and Optimization of the Nutritional Status in Patients With Head and Neck Tumors During and After Radio(Chemo)Therapy

Study ID: NCT06367257

Study Description

Brief Summary: Patients with head and neck cancer requiring definitive or adjuvant radio(chemo)therapy can take part in the study. The aim is to record the nutritional status and diet of the patients during the trial and regularly at a period of 8 weeks after irradiation and to reduce the rate of weight loss and malnutrition.

Detailed Description: Patients with head and neck cancer requiring definitive or adjuvant radio(chemo)therapy can take part in the study. The aim is to record the nutritional status and diet of the patients during the trial and regularly at a period of 8 weeks after irradiation and to reduce the rate of weight loss and malnutrition. Patients in the experimental arm receive the daily reminder message via app (Emento) that they should pay attention to adequate caloric intake. In addition, these patients receive 3 screening questions about their current health and nutritional status twice a week. In case of relevant deterioration (any negative value in the screening questions is explained under study procedure), additional further questions are asked, which are specifically aimed at the side effects of the tumor therapy (mainly dysphagia, pain). The answers will be transmitted to the radiation clinic. If a question is answered positively, this is reported to the radiotherapy clinic on the one hand and on the other hand, the patient is asked to consult the doctor in the clinic as soon as possible.

Keywords

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Universitätsklinikum Erlangen, Strahlenklinik, Erlangen, Bavaria, Germany

Contact Details

Name: Marlen Haderlein, PD

Affiliation: Universitätsklinikum Erlangen, Radiation Oncology

Role: STUDY_DIRECTOR

Name: Luitpold Distel, Prof.

Affiliation: Universitätsklinikum Erlangen, Radiation Oncology

Role: STUDY_DIRECTOR

Name: Allison Lamrani

Affiliation: Universitätsklinikum Erlangen, Radiation Oncology

Role: PRINCIPAL_INVESTIGATOR

Name: Charlotte Schmitter, Dr.

Affiliation: Universitätsklinikum Erlangen, Radiation Oncology

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

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