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临床试验/NCT06407570
NCT06407570尚未招募不适用

Dysphagia and Quality of Life in Patients With Oral Squamous Cell Carcinoma Before and After Treatment

University of Aarhus1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2024年6月1日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
100
试验地点
1
主要终点
Days alive and out of hospital

研究概览

简要总结

While the group of oral cavity cancer (OCC) survivors continue to increase, surgeons and oncologist intensify their search for improved treatment and rehabilitation methods to reduce the morbidity of management without compromising the oncological safety. The predominant problem after treatment of OCC is dysphagia, which is associated with malnutrition, aspiration pneumonia, hospital re-admission, and reduced quality of life (QoL) and survival.

In a pilot study, the investigators found that 45% of OCC patients reported significant eating disabilities two years after surgical treatment. However, the international literature is limited on the dysphagia and QoL of OCC survivors.

With an overall goal to improve the QoL and health status in patients treated for OCC, the present study aims to

  1. systematically evaluate the swallowing function before and after treatment,
  2. investigate the impact of swallowing function on QoL,
  3. identify risk factors for dysphagia,
  4. investigate if swallowing function is an independent factor for the number of ´days alive and out of hospital´
  5. evaluate the rehabilitation offered to OCC patients in Danish municipalities and the effect on swallowing outcomes.

One hundred patients treated for OCC will be included prospectively during a 2-year period. Data on type and location of tumour, treatment modality, complications, patient weight, dietary intake, rehabilitation program, hospital admissions, recurrences, and survival will be collected. Questionnaires and Modified Barium Swallow Study (MBSS) will be performed before and 2 and 12 months after treatment.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Histologically confirmed squamous cell carcinoma with any location in the oral cavity including recurrences. Patients will only be included once
  • Treatment with curative intent (surgery and/or (chemo)radio therapy)

排除标准

  • Allergy to barium contrast
  • Pregnancy or breastfeeding
  • Inability or unwillingness to complete questionnaires and undergo examinations

结局指标

主要结局

Days alive and out of hospital

时间窗: 12 months post-operative

During regular outpatient follow-up, the patient will be asked about hospital admission/re-admission since the last visit and the electronic chart will be accessed for verification of reason and length of stay.

MD Anderson Dysphagia Inventory (MDADI)

时间窗: Baseline, 2 and 12 months post-operative

The MDADI is a 20-item questionnaire assessing dysphagia-related QoL in head and neck cancer patients covering global, emotional, functional, and physical domains. The score ranges from 20 (poor function) to 100 (high function). The patient answers the questionnaire assisted by a nurse. A 10-point difference between groups in composite score is considered significant.

Modified Barium Swallow Impairment profile (MBSImp)

时间窗: Baseline, 2 and 12 months post-operative

MBSImp is a 17-point assessment tool (0-55 points, a higher score indicates worse swallowing function) for interpreting MBSS that includes evaluation of the oral, pharyngeal and esophageal phase. The Penetration/Aspiration Scale will be applied for evaluating swallow safety ranging from 1 (no penetration/aspiration) to 8 (silent aspiration). The recordings as well as the interpretations are carried out by one of two trained otorhinolaryngologists.

次要结局

  • Weight(Baseline, 2 and 12 months post-operative)
  • European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire Head And Neck 35 (EORTC H&N-35)(Baseline, 2 and 12 months post-operative)
  • European Organisation for Research and Treatment of Cancer Quality of Life Questionnaire C30 (EORTC QLQ-C30)(Baseline, 2 and 12 months post-operative)
  • Functional oral intake score (FOIS)(Baseline, 2 and 12 months post-operative)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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