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Qualitative Exploration of Head & Neck Cancer Patient Reported Experience of Radiotherapy

Qualitative Exploration of Head & Neck Cancer Patient Reported Experience of Radiotherapy With Focus on Restriction Anxiety & 'Claustrophobia

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04543045
Acronym
H&NPRER-RAC
Enrollment
20
Registered
2020-09-09
Start date
2021-05-05
Completion date
2023-09-30
Last updated
2023-03-14

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

Conditions

Anxiety, Head and Neck Cancer, Oncology

Keywords

patient experience, claustrophobia, radiotherapy, radiotherapy moulds, radiotherapy masks

Brief summary

The study aims to explore the experience of patients with Head and Neck Cancer, who are preparing for and/or completed radiotherapy treatment.

Detailed description

This is a non-interventional study using interviews to explore head and neck cancer patients' experience of preparing for and completing radiotherapy utilising an immobilisation mask. The study will be conducted in 2 stages: The first stage is Item generation. Approximately 20 interviews will be conducted with head and neck cancer patients who have completed or partially completed radiotherapy. The interviews will capture their experiences and views pertaining to mould making, scans and radiotherapy, reported associated fear of restriction, suffocation, loss of control and fear of public embarrassment during treatment. The data from the interviews will be used to develop potential items for a screening tool for identification of those patients likely to experience anxiety and claustrophobia before they start their treatment. The second stage is cognitive interviews. Approximately 5 patients included in Stage I will be invited to take part in a further interview to review the themes and potential questionnaire items identified from interviews.

Interventions

not an intervention

Sponsors

The Christie NHS Foundation Trust
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
RETROSPECTIVE

Eligibility

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

Inclusion criteria

* Aged over 18 (no upper age limit) * Completed or partially completed radiotherapy treatment utilising a mask ≥ 6 weeks previous to study entry

Exclusion criteria

* Unable to understand and communicate in the English language * Unable to provide written informed consent

Design outcomes

Primary

MeasureTime frameDescription
Patient experiencewithin 6 weeks of using a maskInterviews will be used to generate themes that capture the patients experience. These themes are the primary outcome.There are no units of measurement or data collection tools only an interview schedule.

Secondary

MeasureTime frameDescription
potential items for a questionnaire2 months after completing or partially completing radiotherapy.interviews extracts will be used as potential item for the interview

Countries

United Kingdom

Contacts

Primary ContactDaisy Hopper
daisy.hopper@nhs.net

Outcome results

None listed

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