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CompletedNCT00533663Updated Jun 23, 2022

Healing Touch During Chemotherapy Infusions for Women With Breast Cancer

An interventional study of Healing Touch and Standard care in Breast Cancer, sponsored by Stanford University. Completed at 1 site in United States. Open to female participants aged 18 Years to 70 Years. Per ClinicalTrials.gov, last updated 2022-06-23.

Sponsored by Stanford University · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
32
Allocation
Randomized
Ages
18 Years to 70 Years
Sex
Female
01

Study summary

To study if Healing Touch is effective during chemotherapy treatment for breast cancer

Read the detailed description

To study the effectiveness of Healing Touch provided during chemotherapy infusions on the experience of women undergoing treatment for breast cancer. Healing Touch (HT) is a gentle, non-invasive form of energy-balancing work that promotes relaxation and can help manage the side effects of chemotherapy.

02

Conditions studied

  • Breast Cancer

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03

In context

Breast Neoplasms

12,544 studies on the registry are indexed under Breast Neoplasms; 2,892 are open to participants now.

This study's enrollment of 32 is below the median of 72 across 9,303 interventional studies indexed under Breast Neoplasms.

Browse Breast Neoplasms studies →

Lead sponsor

Stanford University is the lead sponsor of 2,117 studies on the registry; 425 are open to participants now.

Of its 259 completed or terminated interventional studies of FDA-regulated products, 197 (76%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 70 Years
Sexes eligible
Female
Accepts healthy volunteers
No

Eligibility criteria

Inclusion Criteria:- Stage I or II breast cancer

  • Post-operative
  • Concurrent enrollment on a treatment protocol of 8 weeks of adriamycin + cyclophosphamide given every other week followed by 8 weeks of paclitaxel given every other week
  • ECOG Performance Status: 0 to 2
  • Speak and read English

Exclusion Criteria:- Previous chemotherapy exposure

  • Concomitant energy-work interventions (HT, Reiki, QiGong, acupuncture).
05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Factorial assignment
Masking
None (open label)
Enrollment
32 participants (actual)

Study arms

  • Experimental
    Standard Care + Healing Touch (HT)

    A a gentle, non-invasive form of energy-balancing work that promotes relaxation and can help manage the side effects of chemotherapy. It occurs every other week (during their infusion).

    Procedure: Healing Touch · Other: Standard care

  • Active comparator
    Standard Care + Guided relaxation

    Guided relaxation every other week (during their infusion).

    Other: Standard care · Procedure: guided relaxation

  • Active comparator
    standard care only

    Standard care

    Other: Standard care

Interventions

  • ProcedureHealing Touch

    every other week (during their infusion)

  • OtherStandard care

    Adriamycin, cyclophosphamide, and paclitaxel administered as standard of care

  • Procedureguided relaxation
06

What researchers measure

Primary outcomes

  1. FACT-B summary score

    Time frame: Baseline, 6 wks, 14 wks

Secondary outcomes

  1. Domain scores for FACT-B; BSI-18; FACIT-Fatigue; nausea measured on a Likert scale

    Time frame: Baseline, 6 wks, 14 wks

07

Study locations

1 site
  • Stanford University School of Medicine
    Stanford, California 94305, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Jun 23, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00533663
Lead sponsor
Stanford University
Responsible party
Sponsor
First posted
Sep 21, 2007
Start date
Apr 2007
Primary completion
Aug 2010
Completion
Aug 2010
Last update
Jun 23, 2022

Study contacts

Kathy Turner, RN, NP
principal investigator · Stanford University
Alice "Ellie" Guardino, RN, NP
principal investigator · Stanford University

Oversight

Data monitoring committee
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Jun 2022. You cannot join it, but the record below documents what was studied.

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