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Effects of supportive interventions during postoperative adjuvant radiotherapy on symptoms and functional outcomes in breast cancer

Effects of supportive interventions during postoperative adjuvant radiotherapy on symptoms and functional outcomes in breast cancer

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600127853
Enrollment
Unknown
Registered
2026-07-08
Start date
2024-12-05
Completion date
Unknown
Last updated
2026-07-13

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

Conditions

Breast cancer

Interventions

Control group:Usual radiotherapy nursing care only, including education about the radiotherapy process, skin-care guidance, general activity advice, and routine symptom monitoring. No standardized upp
Rehab group:Standardized upper-limb rehabilitation in addition to usual care, including breathing and postural training, shoulder range-of-motion exercises, scapular stabilization and chest-shoulder f
MusicPMR group:Music-assisted progressive muscle relaxation in addition to usual care. Each session lasts approximately 20-25 minutes and includes breathing adjustment, progressive tension-release rel
Combined group:Standardized upper-limb rehabilitation plus music-assisted progressive muscle relaxation in addition to usual care. Both interventions are delivered according to the procedures describe

Sponsors

Nanping First Hospital Affiliated to Fujian Medical University (Nanping First Hospital)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1.Female patients aged >=18 years and <=70 years. 2.Pathologically confirmed unilateral breast cancer after surgery. 3.Completion of breast-conserving surgery without axillary lymph node dissection, including patients who underwent sentinel lymph node biopsy or no axillary dissection. 4.Scheduled to receive postoperative adjuvant whole-breast radiotherapy and expected to complete the planned radiotherapy course. 5.Well-healed surgical wound without active wound infection. 6.Eastern Cooperative Oncology Group performance status of 0-2. 7.Able to hear, understand, communicate, and cooperate with intervention training, questionnaire completion, and follow-up assessments. 8.Willing to participate in the study and able to provide written informed consent.

Exclusion criteria

Exclusion criteria: 1.Bilateral breast cancer, recurrent breast cancer, or distant metastasis. 2.Previous radiotherapy to the ipsilateral breast or chest wall. 3.Clinically diagnosed moderate-to-severe upper-limb lymphedema before surgery or at baseline. 4.Severe shoulder, cervical spine, or neuromuscular disease that may interfere with upper-limb functional assessment or rehabilitation training. 5.Severe cardiopulmonary disease, uncontrolled hypertension, or other conditions considered unsuitable for rehabilitation training. 6.Severe psychiatric disorder, cognitive impairment, or current participation in structured psychological therapy, music therapy, or relaxation training. 7.Any other condition judged by the investigators to make participation inappropriate.

Design outcomes

Primary

MeasureTime frame
Sleep quality;

Secondary

MeasureTime frame
Upper-limb function;Fatigue;Anxiety;Depression;Pain intensity;Upper-limb stiffness;

Countries

China

Contacts

Public ContactWenzhu Wei

Nanping First Hospital Affiliated to Fujian Medical University (Nanping First Hospital)

842991307@qq.com+86 599 863 8275

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Jul 23, 2026