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Construction and Effectiveness of a Dyadic Coping-Based Intervention for Illness Communication Avoidance in Head and Neck Cancer Patients Undergoing Radiotherapy and Their Spouses

Construction and Effectiveness of a Dyadic Coping-Based Intervention for Illness Communication Avoidance in Head and Neck Cancer Patients Undergoing Radiotherapy and Their Spouses

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600128603
Enrollment
Unknown
Registered
2026-07-22
Start date
2026-08-01
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

Illness Communication Avoidance

Interventions

control group:Routine care
intervention group:illness communication avoidance intervention
Observation group:None

Sponsors

The Clinical Technology Research And Development Center of Shanghai Proton and Heavy Ion Center; Shanghai Proton and Heavy Ion Center (SPHIC)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
20 Years to 80 Years

Inclusion criteria

Inclusion criteria: Patient inclusion criteria: 1. Female patients aged 20 to 80 years and male patients aged 22 to 80 years (in line with the legal marriageable age in China); 2. Diagnosed with HNC by pathology, including primary tumors in the oral cavity, nasal cavity, pharynx, maxillofacial region, salivary glands, and neck; 3. Undergoing radiotherapy with or without concurrent chemotherapy, with a total radiotherapy dose ranging from 40 to 75 Gy (5 fractions per week), and treatment duration of 4 to 7 weeks; 4. Married, and the main caregiver during hospitalization is the spouse; 5. Able to listen, speak, read, write, and correctly understand and answer questions; 6. Informed of the tumor diagnosis, willing to participate in this study and sign the informed consent form. Spouse inclusion criteria: 1. Spouses of HNC radiotherapy patients included in this study; 2. Main caregivers; 3. Good listening, speaking, reading, writing, and communication skills; 4. Informed consent and willingness to participate in the study.

Exclusion criteria

Exclusion criteria: Patient exclusion criteria: 1. In the acute stage of the disease, or with severe liver and kidney function, heart and lung function impairment reaching grade III or above (according to CTCAE v5.0 standards); 2. Diagnosed with severe mental disorders (such as schizophrenia, severe depression with psychotic symptoms, etc.), or with significant cognitive function deficits (such as a Montreal Cognitive Assessment (MoCA) score below 20 points). Spouse exclusion criteria: 1. Cognitive impairment; 2. Life-threatening diseases.

Design outcomes

Primary

MeasureTime frame
illness communication avoidance;

Secondary

MeasureTime frame
intimacy;Adherence to the disease communication avoidance intervention.;dyadic coping;quality of life;

Countries

China

Contacts

Public ContactHongwei Wan

The Clinical Technology Research And Development Center of Shanghai Proton and Heavy Ion Center; Shanghai Proton and Heavy Ion Center (SPHIC)

hongwei.wan@sphic.org.cn+86 21 38296666

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Aug 10, 2026