Skip to content

Patient and Caregiver Preferences for Multimodal Cancer Pain Management Services in Advanced Cancer: A Single-Center Discrete Choice Experiment

Patient and Caregiver Preferences for Multimodal Cancer Pain Management Services in Advanced Cancer: A Single-Center Discrete Choice Experiment

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600129241
Enrollment
Unknown
Registered
2026-08-01
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

Cancer Pain

Interventions

Patient group:None (Non-interventional discrete choice experiment, questionnaire-based survey only)
Family caregiver group:None (Non-interventional discrete choice experiment, questionnaire-based survey only)

Sponsors

West China Hospital of Sichuan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Patient inclusion criteria: 1. Age >=18 years; 2. Diagnosed with malignant tumors through pathology or clinical diagnosis; 3. Patients with advanced cancer, including stage IV, recurrent, or metastatic tumors, or those judged by clinicians as unsuitable for radical treatment; 4. Experiencing cancer pain, defined as a Numeric Rating Scale (NRS) score >=3 in the past week, or currently receiving pain management related to cancer; 5. Able to understand and complete questionnaires; 6. Willing to participate in the study and sign informed consent. Family caregiver inclusion criteria: 1. Age >=18 years; 2. Recognized by the patient as the primary family caregiver; 3. Involved in the patient's daily care, medication management, or medical decision-making; 4. Able to understand and complete questionnaires; 5. Willing to participate in the study and sign informed consent.

Exclusion criteria

Exclusion criteria: Patient Exclusion Criteria: 1. Presence of severe cognitive impairment, delirium, or mental disorder, making it impossible to complete the questionnaire; 2. Extremely unstable condition or deemed by the researcher as unsuitable for participation in the survey; 3. Unable to understand the Chinese questionnaire content; 4. Have already participated in the preliminary survey phase of this study. Family Caregiver Exclusion Criteria: 1. Presence of cognitive or communication impairment, making it impossible to complete the questionnaire; 2. Unable to understand the Chinese questionnaire content; 3. Participation in the survey is deemed by the researcher to potentially cause significant psychological burden or be inappropriate.

Design outcomes

Primary

MeasureTime frame
Relative importance of each attribute of multimodal cancer pain management services (%);

Secondary

MeasureTime frame
Willingness-to-pay (WTP) for each attribute level (CNY);Differences in preferences between patients and family caregivers;Predicted choice probabilities for different service packages;

Countries

China

Contacts

Public ContactBixin Zheng

West China Hospital of Sichuan University

binxin.zheng@scu.edu.cn+86 28 85422337

Outcome results

None listed

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