Skip to content

A study on the construction and efficacy of illness perception intervention program for colorectal cancer patient-spousal caregiver dyads

A study on the construction and efficacy of illness perception intervention program for colorectal cancer patient-spousal caregiver dyads - A study on illness perception intervention program for colorectal cancer patient-spousal caregiver dyads

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400082920
Enrollment
Unknown
Registered
2024-04-11
Start date
2024-04-15
Completion date
Unknown
Last updated
2024-04-15

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

Conditions

Colorectal cancer

Interventions

Intervention group:Combining face-to-face and telephone, the intervention program employed approaches of knowledge disease guidance, psychological education and skill training. The themes of six inter
Control group:Usual care

Sponsors

Jiangnan University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: ? One of the couples was diagnosed with colorectal cancer (any diagnosed) by pathological diagnosis; ? The spouses was the primary caregiver of the patient; ? Adults married couples (age >18 years old); ?Neither patient nor spousal caregiver have a verbal communication disorder and cognitive impairment (such as bipolar disorder, Alzheimer's disease, etc.), and can communicate normally; ? Both partners of the couple have basic reading, understanding and writing skills, and can cooperate with the teaching of the intervention content; ? At least one of the spouses has a mobile phone, and can use the mobile phone to answer or chat on Wechat; ? Both partners of the couple have informed consent and volunteered to participate in the study; ? Both partners of the couple are aware of the illness and have the capacity for civil conduct.

Exclusion criteria

Exclusion criteria: ? The spouse was not the primary informal caregiver of the patient; ? Spousal caregivers have serious physical or psychological diseases, such as severe depression; ? Either partner was unable or unwilling to participate in the program.

Design outcomes

Primary

MeasureTime frame
Illness perception;

Secondary

MeasureTime frame
Dyadic coping;Marital satisfaction;Anxiety and depression;Quality of life;

Countries

China

Contacts

Public ContactQiuping Li

Jiangnan University

Liqp@163.com+86 189 1529 9739

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026