Research on New Methods and New Models of Rehabilitation Intervention for Cancer Patients Based on Exercise and Psychological Intervention

NCT ID: NCT07317765

Last Updated: 2026-01-05

Basic Information

• Recruitment Status: ACTIVE_NOT_RECRUITING
• Clinical Phase: NA
• Total Enrollment: 200 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2025-03-17
• Study Completion Date: 2025-12-30

Brief Summary

A Randomized Controlled Trial of Natural Psychotherapy for Intervening Negative Emotions in 100 Breast Cancer Patients

Conditions

Breast Cancer

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: SINGLE

Study Groups

intervention group

Group Type: EXPERIMENTAL

Natural Psychotherapy

Intervention Type: OTHER

A short-term psychological intervention of natural psychotherapy will be conducted for breast cancer patients over a five-week period, using a hybrid online and offline format. The first intervention session will be delivered offline, followed by online video-based sessions thereafter.

control group

Group Type: OTHER

Receive routine psychotherapy and read popular science materials related to breast cancer.

Intervention Type: OTHER

This intervention (routine psychotherapy plus breast cancer popular science materials) is used in control group studies for data comparison purposes, serving as a baseline to evaluate the efficacy of the experimental intervention

Interventions

Natural Psychotherapy

A short-term psychological intervention of natural psychotherapy will be conducted for breast cancer patients over a five-week period, using a hybrid online and offline format. The first intervention session will be delivered offline, followed by online video-based sessions thereafter.

Intervention Type: OTHER

Receive routine psychotherapy and read popular science materials related to breast cancer.

This intervention (routine psychotherapy plus breast cancer popular science materials) is used in control group studies for data comparison purposes, serving as a baseline to evaluate the efficacy of the experimental intervention

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• Patients with pathologically confirmed breast cancer, no distant metastasis, who have completed the perioperative period and not received subsequent treatment;
• Aged 18-59 years with an expected survival period of ≥ 1 year;
• Breast cancer patients with a self-reported depression score of ≥ 53 and/or anxiety score of ≥ 50 on self-rating scales (e.g., Self-Rating Depression Scale [SDS], Self-Rating Anxiety Scale [SAS]);
• Voluntarily participating in the study after providing informed consent and signing the informed consent form.

Exclusion Criteria

• Patients with advanced breast cancer (stage IV with distant metastasis);
• Patients receiving other psychological interventions besides this study (e.g., individual counseling, group therapy);
• Patients with severe mental illness (e.g., schizophrenia), cognitive impairment (MMSE score < 24), heart disease, severe physical illness, other cancers, or complications;
• Patients who are unable to cooperate with psychological interventions, questionnaires, or interviews; patients who request or voluntarily withdraw from this study.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 59 Years
• Eligible Sex: FEMALE
• Accepts Healthy Volunteers: Yes

Sponsors

Beijing HuiLongGuan Hospital

OTHER

Sponsor Role: lead

Responsible Party

Xiang Yang Zhang

Professor

Responsibility Role: PRINCIPAL_INVESTIGATOR

Locations

San Huan Cancer Hospital

Beijing, Beijing Municipality, China

Countries

China

Other Identifiers

2022-2G-4029

Identifier Type: -

Identifier Source: org_study_id