- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05386225
Individualized Follow-Up for Head and Neck Cancer (INFLUENCE)
Study Overview
Status
Conditions
Detailed Description
Background of the study:
Head and Neck Cancer (HNC) patients are currently enrolled in routine follow-up by medical specialists (standardized follow-up) for five years after primary treatment, according to the Dutch guideline Head and Neck Tumors. Similar recommendations are described in guidelines from the US and UK. The purposes for aftercare following cancer treatment as stated by the Health Council of the Netherlands are to address the effects of the disease and treatment itself, to detect new cancer manifestations, and to evaluate medical procedures to improve the quality of care.
The majority of HNC recurrences occur in the first 1.5-two years after treatment, and most of them cause clinical symptoms.It has not been proven that patients with recurrent disease discovered in the asymptomatic phase have better treatment options and life expectancy than patients who experience symptoms at the time of discovery.
Detecting second primary tumors (SPT) is an extra argument for routine follow-up as HNC patients are at greater risk of developing second primary cancers. SPTs are known to negatively affect overall long-term survival, especially those found outside the head and neck area. However, the way in which control visits are performed, namely physical examination of the head and neck, does not aim to identify SPTs elsewhere in the body. Because the incidence of SPTs remains stable over the years after treatment, detecting them would require life-long follow-up through diagnostic imaging.
Many patients express the concern that their cancer will progress or recur after treatment, also known as fear of cancer recurrence (FCR). FCR has a major impact on quality of life. It is not clear whether routine control visits exacerbate or relieve FCR, although previous research suggests that patient-led follow-up, in which prescheduled visits are replaced by patient-education and access to care by self-referral, does not influence FCR. Furthermore, patients have reported being anxious before scheduled control visits.
Overall, de-intensifying routine follow-up after primary HNC treatment seems to be sensible in the light of discovering recurrent or new cancers and will probably not affect FCR. However, reducing the frequency of prescheduled control visits for all HNC patients may deny the varying needs of individual patients. These needs include receiving more information about the treatment trajectory and being more involved in the decision-making process. Therefore, we have implemented a novel decision-aided follow-up program that allows HNC patients to choose between continuing standardized follow-up with prescheduled control visits, and individualized follow-up with symptom-based visits.
Objective of the study:
The aim of this project is to evaluate implementing the choice for individualized follow-up after head and neck cancer treatment at the Radboudumc and Rijnstate, the preferred partner of the Radboudumc regarding head and neck oncology. It will be investigated to what extent it is feasible to offer patients the choice for individualized follow-up, 1.5 years after completion of treatment. In addition, insight into (cost-)effectiveness is explored.
Primary research question: What is the feasibility of offering head and neck cancer patients the choice between standardized and individualized follow-up in a shared-decision making process supported by a decision-aid after completing 1.5 years of standardized follow-up?
Secondary research questions:
- How many patients choose individualized follow-up after completing 1.5 years of standardized follow-up if they are supported by a decision-aid and their treating physician in a shared-decision-making process?
- To what extent do patients who choose individualized follow-up differ from patients who choose standardized follow-up, based on gender, age, educational level, or other patient- or tumor characteristics?
- What are patients' experiences with the choice in terms of the decision-making-process and decisional regret?
- What are physicians' experiences with the choice in terms of the decision-making-process?
- What is the effect of this choice on fear of cancer recurrence and other quality of life outcome measures?
- What is the difference in costs between standardized and individualized follow-up?
- Is there a difference in timing and manner of detection of recurrences between patients who opted for standardized and individualized follow-up? We hypothesize that giving patients the choice between standardized and individualized follow-up is feasible and has a positive effect on FCR, while maintaining QoL and reducing medical costs. We do not expect to diagnose less recurrences or second primary tumors in patients who opted for individualized follow-up.
Study design:
This is an observational study (prospective cohort study) to evaluate offering a choice for individualized follow-up after treatment for HNC in Radboudumc and Rijnstate.
Study population:
Patients with a primary malignancy in the head and neck region (nose, nasopharynx, nasopharynx, oral cavity, pharynx, larynx) who have undergone treatment with curative intent.
Introducing individualized follow-up:
All head and neck cancer patients who are enrolled in standardized follow-up will be informed on the choice between standardized and individualized follow-up directly after treatment. Patients who have completed 1.5 years of standardized follow-up will be asked to make a choice between continuing standardized follow-up or switching to individualized follow-up. Patients will gain access to our online decision-aid to support the decision-making process. Their treating physician will explain all the details during a decision-making consult, after which a decision is made.
Including participants:
Patients who are eligible to participate in this study will be scheduled for an outpatient visit with an independent researcher 1.5 years after treatment, regardless of their choice for standardized or individualized follow-up. The researcher will explain the study and study-goals. Another appointment will be scheduled two weeks later to answer possible questions and, if the patient is willing to participate, obtain informed consent.
Ethical aspects:
We expect that patients who are given the opportunity to choose their own form of follow-up will not regret their decision. Nevertheless, participants always have the option to withdraw their decision at any time during the study, and afterwards. Participants in this study will not receive any special compensation or reward.
Data management:
All participants who have given informed consent are assigned an identification code. The identification code is copied on the code list. Identifiable data of the included study participants are kept in the code list (name, address, telephone number, medical file number (MDN), etc.). No traceable data are recorded in the electronic database (Castor EDC), only the participant's identification code. The code list is kept in a separate and secured digital environment.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Cecile van de Weerd, MD
- Phone Number: 0031243614933
- Email: cecile.vandeweerd@radboudumc.nl
Study Locations
-
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Gelderland
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Nijmegen, Gelderland, Netherlands, 6525 GA
- Recruiting
- Radboud University Medical Center
-
Contact:
- Cecile van de Weerd, MD
- Email: cecile.vandeweerd@radboudumc.nl
-
Principal Investigator:
- Robert Takes, Prof
-
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Malignant tumor of the head and neck
- First primary HNC
- Participant was treated with curative intent
- Participant has completed one year of uncomplicated routine follow-up
- Treating physician supports the possible choice for patient-led follow-up
Exclusion Criteria:
- Malignant tumors of salivary glands
- Participant is cognitively impaired
- Participant is unable to read or write in Dutch
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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Standardized follow-up
Participants who chose to continue guideline-prescribed, standardized follow-up one year after HNC treatment.
|
Individualized follow-up
Participants who chose to switch to individualized follow-up one year after HNC treatment.
Follow-up visits will only be scheduled based on clinical symptoms and questions, initiated by the patient.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Follow-up decision
Time Frame: Baseline
|
The type of follow-up that was chosen (standardized or individualized) will be distracted from the electronical patient record.
|
Baseline
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Demand - assessed by the reach
Time Frame: 1.5 years
|
Number of patients who received the decision-aid and the choice for follow-up in our clinical practice divided by the number of patients eligible to use the decision-aid and thus make a choice between the two follow-up programs.
|
1.5 years
|
Acceptability - assessed by the SUS
Time Frame: Baseline
|
The use of the decision-aid will be evaluated using the System Usability Scale (SUS): 10 items giving a global view of subjective assessments of usability of the decision-aid on a 5-point scale from strongly disagree (1) to strongly agree (5).
A higher score means higher usability.
10 self-constructed questions about the presentation, actual use, and perceived added value are added to the questionnaire.
|
Baseline
|
Tailored decision aid - usability
Time Frame: Baseline
|
The use of a tailored decision aid to support the decision making process will be evaluated using the System Usability Scale (SUS): 10 items giving a global view of subjective assessments of usability of the decision-aid on a 5-point scale from strongly disagree (1) to strongly agree (5).
|
Baseline
|
Tailored decision aid - use and added value
Time Frame: Baseline
|
The use of a tailored decision aid to support the decision making process will be evaluated by a self-constructed questionnaire consisting of 10 additional questions about the presentation, actual use, and the perceived added value of the decision aid from a patient perspective.
A higher score means higher usability.
|
Baseline
|
Tailored decision aid - implementation in clinical practice
Time Frame: 1.5 years
|
The use of a tailored decision aid from a physician perspective will be evaluated by an adjusted version of the MIDI questionnaire to measure determinants associated with successful implementation of the decision aid.
In general, a higher score means higher (expected) use in clinical practice.
|
1.5 years
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Quality of life - Fear of cancer recurrence
Time Frame: Baseline
|
Fear of cancer recurrence is measured using the Cancer Worry Scale (CWS): 6 items on worries after cancer treatment rated on a 4-point scale from almost never/not at all (1) to almost always/very much (4).
A high score means higher FCR.
|
Baseline
|
Quality of life - EORTC QLQ C-30
Time Frame: Baseline
|
Quality of life is measured using the European Organization for Research and Treatment of Cancer 30-item core quality of life questionnaire (EORTC QLQ C-30): 30 items organized in 5 functional scales (physical, role, emotional, cognitive, social), 3 symptom scales (pain, fatigue, emesis), and a global health and QoL scale rated on a scale from 0 to 100 (100 meaning perfect quality of life for functional scales or heavy burden for symptom scales).
|
Baseline
|
Quality of life - EORTC QLQ-H&N35
Time Frame: Baseline
|
Quality of life is measured using the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire module for patients with head and neck cancer (EORTC QLQ-H&N35): 7 multi-item scales (pain, swallowing, senses, speech, social eating, social contact, sexuality) and 11 single items (teeth, mouth opening, dry mouth, sticky saliva, coughing, feeling ill, use of pain killers, nutritional supplements, feeding tube, weight loss and weight gain) rated on a scale from 0 to 100.
|
Baseline
|
Quality of life - EQ-5D-5L
Time Frame: Baseline
|
Quality of life is measured using the EuroQuality of Life Five Dimensions (EQ-5D-5L) questionnaire, consisting of descriptive health status and visual health status. Descriptive health status: 5 dimensions (mobility, self-care, usual activities, pain/discomfort, anxiety/depression) rated from 1 (no problems) to 5 (extreme problems). Visual health status: visual analogue scale (VAS) from 'worst health you can imagine' - 'best health you can imagine'. |
Baseline
|
Quality of life - Fear of cancer recurrence
Time Frame: 1.5 years
|
Fear of cancer recurrence is measured using the Cancer Worry Scale (CWS): 6 items on worries after cancer treatment rated on a 4-point scale from almost never/not at all (1) to almost always/very much (4).
A high score means higher FCR.
|
1.5 years
|
Quality of life - QLQ C-30
Time Frame: 1.5 years
|
Quality of life is measured using the European Organization for Research and Treatment of Cancer 30-item core quality of life questionnaire (EORTC QLQ C-30): 30 items organized in 5 functional scales (physical, role, emotional, cognitive, social), 3 symptom scales (pain, fatigue, emesis), and a global health and QoL scale rated on a scale from 0 to 100 (100 meaning perfect quality of life for functional scales or heavy burden for symptom scales).
|
1.5 years
|
Quality of life - QLQ-H&N35
Time Frame: 1.5 years
|
Quality of life is measured using the European Organization for Research and Treatment of Cancer Quality of Life Questionnaire module for patients with head and neck cancer (EORTC QLQ-H&N35): 7 multi-item scales (pain, swallowing, senses, speech, social eating, social contact, sexuality) and 11 single items (teeth, mouth opening, dry mouth, sticky saliva, coughing, feeling ill, use of pain killers, nutritional supplements, feeding tube, weight loss and weight gain) rated on a scale from 0 to 100.
|
1.5 years
|
Quality of life - EQ-5D-5L
Time Frame: 1.5 years
|
Quality of life is measured using the EuroQuality of Life Five Dimensions (EQ-5D-5L) questionnaire, consisting of descriptive health status and visual health status. Descriptive health status: 5 dimensions (mobility, self-care, usual activities, pain/discomfort, anxiety/depression) rated from 1 (no problems) to 5 (extreme problems). Visual health status: visual analogue scale (VAS) from 'worst health you can imagine' - 'best health you can imagine'. |
1.5 years
|
Shared decision making for patients
Time Frame: Baseline (after decision making consult)
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Shared decision making will be evaluated using the Shared Decision Making Questionnaire (SDM-Q-9) for patients: 9 items on SDM rated on a 6-point scale from completely disagree (0) to completely agree (6) from a patient perspective.
|
Baseline (after decision making consult)
|
Shared decision making for physicians
Time Frame: Baseline (after decision making consult)
|
Shared decision making (routine or patient-led follow-up) will be evaluated using the Shared Decision Making Questionnaire (SDM-Q-9) for physicians: 9 items on SDM rated on a 6-point scale from completely disagree (0) to completely agree (6) from a physician perspective.
|
Baseline (after decision making consult)
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Decisional conflict
Time Frame: Baseline
|
Decisional conflict is measured by the Decisional Conflict Scale (DCS): 16 items considering decisional conflict rated on a 5-point scale from strongly agree (0) to strongly disagree (4).
A high score means higher decisional conflict.
|
Baseline
|
Decisional regret
Time Frame: 1.5 years
|
Decisional regret is measured by the Decisional Regret Scale (DRS): 5 items considering decisional regret rated on a 5-point scale from strongly agree (0) to strongly disagree (4).
A high score means higher decisional regret.
|
1.5 years
|
Practicality - Medical consumption
Time Frame: Baseline
|
Medical consumption will be measured using the iMedical Consumption Questionnaire (iMCQ): 31 items to assess patient reported general medical consumption (primary and secondary care, including medicine use).
|
Baseline
|
Practicality Medical consumption
Time Frame: 1.5 years
|
Medical consumption will be measured using the iMedical Consumption Questionnaire (iMCQ): 31 items to assess patient reported general medical consumption (primary and secondary care, including medicine use).
|
1.5 years
|
Practicality - Productivity loss
Time Frame: Baseline
|
Productivity loss will be measured using the iProductivity Cost Questionnaire (iMCQ): 18 items to assess patient reported productivity losses in hours (considering absenteeism, presenteeism, and unpaid work).
|
Baseline
|
Practicality - Productivity loss
Time Frame: 1.5 years
|
Productivity loss will be measured using the iProductivity Cost Questionnaire (iMCQ): 18 items to assess patient reported productivity losses in hours (considering absenteeism, presenteeism, and unpaid work).
|
1.5 years
|
Practicality - outpatients visits and tests
Time Frame: 1.5 years
|
The number of outpatient visits and diagnostic tests during the follow-up year after the choice for individualized or standardized follow-up will be collected from the electronical patient record.
|
1.5 years
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Sociodemographic and basic clinical characteristics - input variables
Time Frame: Baseline
|
Patient records: date of birth, sex, primary treatment hospital, date of diagnosis, clinical and pathological tumor characteristics, date and type of primary treatment. Patient reported: living situation, educational level, employment, smoking, alcohol consumption. |
Baseline
|
Oncological outcomes
Time Frame: 1.5 years
|
In case of recurrent/second primary tumor(s) during the study period, the following will be retrieved from the patient record: date of diagnosis, clinical and pathological characteristics, date and type of treatment.
|
1.5 years
|
Collaborators and Investigators
Collaborators
Investigators
- Principal Investigator: Robert P Takes, Prof, Radboud University Medical Center
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 112491
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
IPD Sharing Time Frame
IPD Sharing Access Criteria
IPD Sharing Supporting Information Type
- STUDY_PROTOCOL
- SAP
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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