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The effect of AI-HEALS intervention based on the Fogg Behavior Model on self-management in postoperative breast cancer patients: a randomized controlled trial protocol

The effect of AI-HEALS intervention based on the Fogg Behavior Model on self-management in postoperative breast cancer patients: a randomized controlled trial protocol

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600126533
Enrollment
Unknown
Registered
2026-06-10
Start date
2026-06-10
Completion date
Unknown
Last updated
2026-06-15

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

Conditions

Self-health management in postoperative breast cancer patients involves complex rehabilitation needs (including functional exercise of the affected limb, adherence to endocrine therapy, psychological adjustment, etc.), the physical and psychological burden of long-term treatment, and the adaptive stress experienced during the process of returning to social roles.

Interventions

AI HEALS group:Based on routine nursing care, the intervention was implemented using the intelligent AI-HEALS health education platform, following the principles of
Control group:Routine nursing care

Sponsors

The Fourth Central Hospital of Baoding City
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Female, aged >=18 years; 2.Patients with clinically and pathologically diagnosed stage I–III breast cancer who have undergone surgery and are receiving adjuvant therapy such as radiotherapy or chemotherapy; 3.No history of severe mental health problems, such as a diagnosis of depression or anxiety; 4.Possess basic reading and comprehension skills, and be able to use the WeChat function on a mobile phone independently or with the assistance of a family member; 5.Provide informed consent and voluntarily participate in this study.

Exclusion criteria

Exclusion criteria: 1.Presence of other malignant tumors or definite distant metastasis; 2.Presence of severe cognitive impairment, severe mental disorders, or communication difficulties; 3.Presence of severe dysfunction of vital organs such as the heart, brain, liver, or kidneys that would preclude completion of the study; 4.Unwillingness or inability to use WeChat for daily communication and data recording; 5.Currently participating in other intervention programs or clinical trials that may affect the outcomes of this study; 6.Determined by the investigator to be unsuitable for participation in this study.

Design outcomes

Primary

MeasureTime frame
Cancer Self-Management Assessment Scale;

Secondary

MeasureTime frame
PHQ-4;C-SUPPH;FCRQ7;FACT-B;Comparison of prognosis;FoP-Q-SF;

Countries

China

Contacts

Public ContactHuitao Wang

The Fourth Central Hospital of Baoding City

3591402147@qq.com+86 312 6413166

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jun 21, 2026