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Preoperative Massage in Breast Surgery Patients

Utility of Preoperative Massage in Breast Surgery Patients

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01667328
Enrollment
299
Registered
2012-08-17
Start date
2012-06-30
Completion date
2018-03-19
Last updated
2018-05-03

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

Conditions

Anxiety, Breast Cancer, Presurgical Anxiety

Keywords

Anxiety, Presurgical anxiety, Breast Cancer

Brief summary

This randomized controlled interventional study is designed to determine whether breast cancer surgical patients receiving presurgical massage therapy performed by a licensed massage therapist have decreased average anxiety levels compared to the control group of breast cancer surgical patients who do not receive massage therapy.

Interventions

PROCEDUREMassage therapy

Presurgical 15 minute massage performed by a licensed massage therapist

PROCEDUREStandard of care

Control group will receive standard of care with no massage therapy

Sponsors

Health Quest Systems
CollaboratorUNKNOWN
Dyson Center for Cancer Care
CollaboratorUNKNOWN
Vassar Brothers Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Male or female * Must speak English * Able to give consent * 18 years of age or older * Undergoing first procedure outpatient breast/axillary surgery at Vassar Brothers Medical Center

Exclusion criteria

* Anxiolytics or antidepressants medications during the previous 24 hours * Any condition that would prohibit receiving a massage * IV medications prior to presurgical holding VAS assessment

Design outcomes

Primary

MeasureTime frameDescription
Anxiety levelUpon arrival at the hospital for scheduled surgery and again immediately prior to surgery. Expected interval between measurements estimated to be less than 120 minutes.Assessments will be done immediately post registration and immediately prior to surgery

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026