Home-Based Symptom Management Via Reflexology for Breast Cancer Patients

Not Applicable

Completed

Conditions: Breast Cancer

Interventions: Other: Reflexology

Registration Number: NCT01582971

Lead Sponsor: Michigan State University

Brief Summary: The purpose of this project is to test foot reflexology delivered by a friend or family member in the home for women with breast cancer. The primary aims of the proposed study in a sample of women with breast cancer receiving chemotherapy and/or hormonal therapy are to determine the effects of 4 family- or friend-delivered weekly reflexology sessions compared to an attention control group.

Detailed Description: This project tests the benefits of a home-based intervention of foot reflexology for improving health-related quality of life (HRQOL) including symptom responses, functioning, and health perceptions in women treated with chemotherapy for advanced breast cancer. Reflexology applies a firm walking-motion during sessions and is based on the premise that the foot has reflexes mirroring organs of the body. Symptom burden is the strongest predictor of HRQOL for cancer patients. This project brings together expertise from nursing, reflexology, communication, statistics, and health economics. The primary specific aims, in a sample of women with advanced breast cancer receiving chemotherapy, are to determine the effects of a 4-week, home-based reflexology intervention delivered by a friend/family provider compared to attention control for improvement of:

1. HRQOL including symptoms, functioning, and health perception at study weeks 5 and 11.

The investigators hypothesize that the reflexology group will have better HRQOL (symptoms, functioning, and health perception) than the attention control group at study weeks 5 and 11.

2. Multiple symptom responses and times-to-response as determined by weekly symptom assessments during the 4-week intervention time.

The investigators hypothesize that the reflexology group will have a higher proportion of symptoms that respond to the intervention and shorter time-to-symptom-responses than the attention control group.

3. Symptom-related use of unscheduled health services during the 11-week study. The investigators hypothesize that fewer unscheduled services will be used for symptom management over the 11-week study period by women receiving reflexology compared to women in the attention control.

The exploratory aims are to: 1) Explore differences between trial arms in perceptions of social support due to the family- or friend-delivered reflexology sessions at study weeks 5 and 11; 2) Determine if effects of the reflexology intervention on HRQOL are mediated by social support; and 3) Use the newly developed NIH PROMIS standardized symptom and functioning instruments to assess the effects of the reflexology intervention and to compare the responsiveness of PROMIS instruments and existing instruments designed to measure similar constructs.

This project has immense potential to make an effective symptom management intervention accessible to patients in their homes via a friend or family home provider. The investigators will not only intervene to enhance HRQOL but also to evaluate social support and costs associated with unscheduled health services. Effective symptom management provides time and cost savings to clinicians, advances the current state-of-the-science, and promotes adherence to medical treatment that may ultimately enhance survival.

Recruitment & Eligibility

Status: COMPLETED

Sex: Female

Target Recruitment: 256

Inclusion Criteria

Age ≥ 21
Diagnosis of breast cancer, Stage III, IV, or Stage I or II with metastasis or recurrence
Able to perform basic ADLs
Undergoing chemotherapy and/or hormonal therapy for breast cancer
Able to speak and understand English
Have access to a telephone
Able to hear normal conversation
Cognitively oriented to time, place, and person (determined via nurse recruiter)

Exclusion Criteria

Diagnosis of major mental illness on the medical record and verified by the recruiter
Residing in a nursing home
Bedridden
Currently receiving regular reflexology
Diagnosis of symptoms of deep vein thrombosis or painful foot neuropathy, which will require medical approval

Study & Design

Study Type: INTERVENTIONAL

Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Intervention	Reflexology	Reflexology: 4 weekly foot reflexology sessions delivered by friend/family member

Primary Outcome Measures

Name	Time	Method
Patient Reported Outcomes Measurement Information System (PROMIS) V 1.0	Week 5 and week 11	1. PROMIS-Physical functioning subscale contains four items. Score for each item ranging from 1 to 5, yielding a total score ranges from 4 to 20. Raw score is converted to a T-score using PROMIS scoring rules. The T-scores have mean 50 and standard deviation 10 for the general population. 2. PROMIS-Satisfaction with participation in social roles subscale contains four items. Score for each item ranges from 0 to 4, yielding a total score ranges from 0 to 16. Raw score is converted to a T-score using PROMIS scoring rules. The T-scores have mean 50 and standard deviation 10 for the general population. Higher scores representing better outcomes in each subscale.
Quality of Life Index (QLI)	Week 5 and week 11	The QLI assesses perceived quality of life including health and functioning domain, psychological/spiritual domain, social and economic domain, and family domain. The QLI consists of two sections: one measures respondent's satisfaction with the various domain of life and the other measures the importance of those domains. The satisfaction scores are centered and weighed by the importance scores to obtain the QLI composite score that ranges from 0 to 30 with higher scores representing better outcomes.
Use of Unscheduled Health Service	Week 11	Measured by Conventional Health Service and Productivity Costs to assess the number of unscheduled times the patient visits an emergency room, urgent care center, and hospitalization.
The M.D. Anderson Symptom Inventory (MDASI)	Week 5 and week 11	The M.D. Anderson Symptom Inventory (MDASI) evaluates severity of 13 symptoms experienced by cancer patients (pain, fatigue, nausea, disturbed sleep, distress, shortness of breath, difficulty remembering, decreased appetite, drowsiness, dry mouth, sadness, vomiting, numbness/tingling) on the scale from 0=symptom not present to 10=as bad as you can imagine. Summed symptom severity score ranging from 0 to 130 was derived. MDASI also assesses how much symptoms interfered with 6 aspects of daily life: general activity, mood, work (including work around the house), relations with other people, walking, and enjoyment of life on the scale from 0=did not interfere to 10=interfered completely. Summed interference score ranging from 0 to 60 was derived. Higher symptom severity and interference scores represent worse outcome.

Secondary Outcome Measures

Name	Time	Method

Trial Locations

Locations (9): Northwestern
🇺🇸
Chicago, Illinois, United States
Hurley Medical Center
🇺🇸
Flint, Michigan, United States
Breslin Cancer Center
🇺🇸
Lansing, Michigan, United States
Sparrow Cancer Center
🇺🇸
Lansing, Michigan, United States
Beaumont Hospital
🇺🇸
Royal Oak, Michigan, United States
Lemmon-Holton Cancer Center
🇺🇸
Grand Rapids, Michigan, United States
McLaren Macomb
🇺🇸
Mount Clemens, Michigan, United States
St. Joseph Mercy Oakland Hospital
🇺🇸
Pontiac, Michigan, United States
St. Johns Providence
🇺🇸
Warren, Michigan, United States