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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT06459245
Other study ID # 2023SF23
Secondary ID
Status Enrolling by invitation
Phase N/A
First received
Last updated
Start date June 15, 2024
Est. completion date September 30, 2024

Study information

Verified date June 2024
Source Peking University First Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Based on the best evidence, this study intends to construct resistance appropriate for this clinical scenario,The training program was designed in a randomized controlled study for patients with breast cancer after surgery for a period of 3 months,To investigate the effect of resistance training on the grip strength of the affected limb, the range of motion of the shoulder joint of the affected limb, the occurrence of lymphedema of the affected limb, and the quality of life of patients with breast cancer after surgery,To provide theoretical guidance and practical basis for functional rehabilitation management of patients with affected limbs after surgery.


Recruitment information / eligibility

Status Enrolling by invitation
Enrollment 30
Est. completion date September 30, 2024
Est. primary completion date September 30, 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years and older
Eligibility Inclusion Criteria: It was first diagnosed as grade I to III unilateral breast cancer by pathological examination. ? Breast cancer surgery was completed and axillary lymph node dissection was performed; ? To receive postoperative adjuvant treatment and follow-up in the outer fourth ward; ? Be able to communicate and exchange normally; ? Volunteer to participate in this research Exclusion Criteria: ? Extreme fatigue, severe anemia, ataxia, etc.; The presence of upper limb or shoulder problems from breast cancer treatment; (3) Edema is in a non-stable stage (stable stage of edema means no treatment for edema in the past 3 months; No inflammation of the upper extremities requiring anti-infective treatment; No change in daily activities; Limb circumference change < 10%) ? Limited limb movement due to trauma, shoulder periarthritis, etc.; ? Limb braking is required for health reasons. ? Patients are lost to follow-up

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Resistance training
Bend the dumbbell, holding one dumbbell in each hand, on the side of the body, bend the arm to lift the dumbbell, front wall and upper arm as close as possible, pause for a moment, and then slowly lower the dumbbell until both arms are completely straight The second section of the dumbbell side flat, straight back, feet standing, arms perpendicular to the side of the body, hands grasp the dumbbell, to the side above the shoulder level, elbow slightly bent, and then put back in place The third section of the dumbbell rowing, feet stand straight, hold the dumbbell, the arm as far back as possible, can feel the upper arm and the waist back is stretched, and then straight back into the preparatory position Section 4: Lift the dumbbell flat in front of you, with your feet open, hold the dumbbell with both hands, extend your arms naturally in front of you, lift the dumbbell to the elbow above shoulder height, stay for 1-2 seconds.

Locations

Country Name City State
China Peking University First Hospital Beijing

Sponsors (1)

Lead Sponsor Collaborator
Yue WANG

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary Lymphedema occurrence Tissue and local edema due to obstruction of lymphatic drainage 3 months after intervention
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