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Prospective Evaluation of Frailty in Patients With Head and Neck Tumors Before Curative Intended Therapy

Prospective Evaluation of Frailty in Patients With Head and Neck Tumors Before Curative Intended Therapy

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06638216
Acronym
PRE-KOVERI
Enrollment
99
Registered
2024-10-15
Start date
2024-10-07
Completion date
2025-06-12
Last updated
2025-08-28

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

Conditions

Head and Neck Cancers

Keywords

Head and Neck Cancer, Frailty, Geriatric Assessment, Radiation, Maxillo-facial Surgery

Brief summary

In a prospective study the fragility of patients with head and neck tumors before the start of curative therapy will be assessed. Primary objective: Fragility is assessed using the G8 questionnaire. Secondary objectives include the assessment of quality of life and financial burden (EORTC-QLQ C30+ H&N43), swallowing function, cardiopulmonary resilience (6-minute walk test) and the patient's wishes regarding a prehabilitation program. Epidemiological and disease-related data is also collected.

Detailed description

In this prospective study patients with a tumor of the head and neck region, that are planned for Surgery or radiotherapy (chemotherapy) will be included. The probability of developing therapy-associated side effects is significantly increased if the patient is already in a limited general condition, also known as fragility, before the therapy. In addition, due to demographic change, the incidence of head and neck tumors will continue to increase, especially in patients of advanced age. Due to their age, other pre-existing conditions and infirmity, they are at a further increased risk of therapy-related side effects In order to improve the care of patients with head and neck tumors, we must first determine how many patients are affected by fragility. In addition, we want to determine influencing factors that are associated with fragility. These include, for example, difficulty swallowing and weight loss. Based on this data, we will then plan the implementation of an intervention study to establish a prehabilitation program.

Interventions

OTHERGeriatric Assessment

Frailty is assessed using the G8 questionnaire. Secondary objectives include the assessment of quality of life and financial burden (EORTC-QLQ C30+ H&N43), swallowing function, cardiopulmonary resilience (6-minute walk test) and the patient's wishes regarding a prehabilitation program. Epidemiological and disease-related data is also collected.

Sponsors

Charite University, Berlin, Germany
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
SCREENING
Masking
NONE

Eligibility

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

Inclusion criteria

* Indication for curative therapy in the case of an initial diagnosis of head and neck tumor disease * Capacity to consent * At least 18 years of age * Sufficient knowledge of the German language

Exclusion criteria

* \- Lack of capacity to consent * Age \<18 years * Severe impairment of walking ability that makes it impossible to perform the 6MWT safely Contraindications for performing a 6MWT: Absolute contraindications\* for the procedure are * unstable angina pectoris * myocardial infarction in the past month. Relative contraindications are * a resting heart rate \> 120/min * systolic blood pressure \> 180 mmHg * a diastolic blood pressure \> 100 mmHg.

Design outcomes

Primary

MeasureTime frameDescription
Frailtyonce prior to surgery or at beginning of radiationAssessment via G8 (Geriatric Screening Tool) questionnaire consists of 8 questions. The score ranges from 0 (poor score) to 17 points (good score), and a score of 11 or lower indicated frailty, whereas a score between 12 and 14 equals pre-frail patients. Patients with a score above 14 are considert non-frail.

Secondary

MeasureTime frameDescription
swallowing functionprior to surgery or beginning of radiationQuestionnaire (M.D. Anderson Dysphagia Inventory), scores range from 20 (poor function) to 100 (high function)
Cardio-pulmonary resilienceprior to surgery or beginning of radiation6-Minute Walk test
EORTC-QLQ C30 questionnaireprior to surgery or at beginning of radiotherapyEORTC-QLQ C30 questionnaire consist of 30 questions with a score range from 0 to 100. Higher scores represents better quality of life, low scores indicating lower quality of life.
Information on current tumor diseaseprior to surgery or beginning of radiationnumber of patients with T1/T2/T3/T4 Tumor Stage and N1/N2/N3 lymphonodal stage
EORTC-H&N43 questionnaireprior to surgery or at beginning of radiotherapyEORTC-H&N43 questionnaires. Scores are from 0 to 100. A high score indicates high level of symptamotology.
Epidemiologic Dataprior to surgery or beginning of radiationDescriptive (e.g. income, alcohol use, smoking status), epidemiologic data is not scored

Countries

Germany

Outcome results

None listed

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