MedPath

Enhancing Head and Neck Cancer Patients’ Experiences of Survivorship

Phase 3
Active, not recruiting
Conditions
Mental Health
Survivorship
Cancer
Quality of Life
Chronic disease self-management
Mental Health - Depression
Cancer - Head and neck
Physical Medicine / Rehabilitation - Other physical medicine / rehabilitation
Registration Number
ACTRN12613000542796
Lead Sponsor
Associate Professor Jane Turner
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Active, not recruiting
Sex
All
Target Recruitment
120
Inclusion Criteria

Patients eligible for this study must have a diagnosis of head and neck cancer and must have undergone treatment at one of the participating sites

*Aged 18 years or over
*Have within the past month completed a defined treatment protocol for cancer of the tongue, mouth, salivary glands. pharynx, the oro-, hypo- and nasopharynx, nasal cavities, middle ear, sinuses or larynx
OR
Within the past month have completed a defined treatment protocol for non-melanoma skin cancers of the head and neck requiring treatment known to cause toxicity (for example, combinations of surgery, radiotherapy or chemotherapy).
*Able to speak and read English
*Physical, cognitive and mental status such that can participate in the study

Exclusion Criteria

*Inability to speak and read English
*Receiving low-toxicity treatment for head and neck cancer (for example laser therapy alone)
*Presence of severe mental, cognitive or physical conditions with would limit the person’s ability to participate in the study, or which require ongoing regular specialist treatment
Advanced disease if life expectancy is considered to be less than 6 months

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Change in patient Quality of Life as measured by the Functional Assessment of Cancer Therapy – Head and Neck (FACT–H&N)[Baseline, 3-month and 6-month follow-ups]
Secondary Outcome Measures
NameTimeMethod
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