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A study on weight management intervention of breast cancer patients in rehabilitation period under the framework of experience-based co-design

A study on weight management intervention of breast cancer patients in rehabilitation period under the framework of experience-based co-design

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400085663
Enrollment
Unknown
Registered
2024-06-14
Start date
2023-10-01
Completion date
Unknown
Last updated
2024-07-08

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

Conditions

Breast cancer

Interventions

intervention group:Experience-based co-design intervention based on"touch points", combining behavior change strategies such as improving self-efficacy, strengthening self-monitoring, reshaping cognit
control group:Routine care

Sponsors

Shanghai University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: Patient interview: 1) age =18 years; 2) diagnosis of breast cancer (stage I-IIIA) ; 3)having surgery,chemotherapy finished over 3 months; 4) BMI =18.5 kg/m2; 5) consent to be interviewed (with or without the option of being photographed) ; 6) no use of weight loss drugs; Caregiver interview: 1) age =18 years; 2) confirmation of a patient with recovered breast cancer who was included in the study; 3) participation in the care of the patient at all times, being familiar with the patient's condition and recovery; including the patient's spouse, relatives or friends; 4) consent to be interviewed (with the option of being photographed) ; Medical staff interview: 1) health care professionals who are involved in the recovery of a breast cancer patient; 2) years of work in the field of care for 5 years or more. Workshop stage: 1) breast cancer, caregiver and medical staff were selected according to the same criteria as above; 2) agreed to participate in the workshop; Intervention stage: 1) age =18 years; 2) diagnosed with breast cancer (stage I-IIIA) ; 3) after surgery, had completed chemotherapy for more than 3 months and was in recovery; 4) BMI =18.5 kg/m2; 5) did not use weight-loss drugs; 6) did not participate in the resistance exercise research project for more than 3 weeks in the past year; and 7) volunteered to participate in this study.

Exclusion criteria

Exclusion criteria: Patients interview stage: 1) having other serious underlying diseases, such as heart disease, hypertension, diabetes, arthritis, and 2) having cognitive dysfunction. Caregiver interview stage: 1) with cognitive impairment. Medical Staff Interview Stage: 1) thinking the patient experience is not important. Workshop stage: 1) having social difficulties or other physical or psychological factors affecting the normal performance of group activities Intervention Stage: 1) having other cognitive disorders; 2) patients with breast cancer recurrence and metastasis (including local or distant metastasis) ; 3) having a history of malignancy other than primary breast cancer; 4) having severe complications such as hypertension and diabetes; 5) having alternative surgical procedures during the intervention, such as breast reconstruction; 6) other diseases affecting participation in exercise or physical activity; and 7) having other arrangements during the intervention period (such as travel, travel, etc.) affecting the normal conduct of the intervention.

Design outcomes

Primary

MeasureTime frame
Weight;BMI;Body fat rate;Muscle mass;

Secondary

MeasureTime frame
Healthy lifestyle score;Patient Health Participation;Fear of recurrence;Psychological resilience;

Countries

China

Contacts

Public ContactZhaohui Geng

Shanghai University of Traditional Chinese Medicine

gengzh200890@163.com+86 152 2195 6608

Outcome results

None listed

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