Supportive Intervention Programs Study



Status:Completed
Conditions:Colorectal Cancer, Cancer, Cancer, Chronic Pain, Other Indications
Therapuetic Areas:Musculoskeletal, Oncology, Other
Healthy:No
Age Range:18 - Any
Updated:8/17/2018
Start Date:June 2011
End Date:July 2013

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Supportive Intervention Programs to Lessen Treatment Related Symptoms

This randomized clinical trial studies the preliminary efficacy of a yoga skills training
(YST) compared to counseling and education (CE) for reducing treatment-related symptoms in
patients with colorectal cancer who are receiving chemotherapy. The YST may reduce fatigue,
other treatment-related symptoms, and improve the quality of life (QOL) of patients with
colorectal cancer. It is not yet known whether YST is more effective then CE in reducing
these outcomes.

OBJECTIVES:

I. To establish the feasibility of implementing a YST among patients undergoing chemotherapy.
This includes the feasibility of implementing yoga in a treatment setting, and patient
recruitment, adherence, and retention.

II. To obtain preliminary data on the efficacy of a YST for reducing fatigue among patients
undergoing chemotherapy.

III. To obtain exploratory data on the impact of a YST on other treatment-related symptoms
(e.g., pain, distress, nausea) and QOL.

IV. To obtain exploratory data on the impact of a YST on potential psychological
(self-efficacy for coping with cancer, response expectancies for symptoms) and physiological
(interleukin [IL]-6 [IL-6], IL-1 Receptor Antagonist [IL-1Ra], tumor necrosis factor- alpha
[TNF-a], soluble TNF receptor I [sTNFRI], C-reactive protein [CRP]) mediators that may
explain the impact of the YST on fatigue.

OUTLINE: Patients (n=20) are randomized to 1 of 2 treatment arms.

ARM I: Patients participate in three 15-minute YST sessions, comprising awareness meditation
practice, movement practice, and breathing practice and relaxation. Patients also receive a
compact disc (CD) recording of a 15-minute YST session and are instructed to practice the YST
at home 4 times weekly.

ARM II: Patients participate in three 15-minute CE sessions, comprising empathic attention
with an interventionist who allows patients to direct the flow of conversation and provides
supportive comments according to standardized procedures. Patients also receive CDs with
recorded information related to coping with colorectal cancer similar in length to the
suggested practice time in Arm I.

The interventions (Week 2, Week 4, Week 6) and assessments (Week 0, Week 4, Week 8) are
implemented during visits for chemotherapy (every two weeks).

Inclusion Criteria:

- Signed protocol specific informed consent

- Are diagnosed with colorectal cancer

- Recruited within 2 weeks of initiating chemotherapy (including reinitiating
chemotherapy after a treatment holiday of greater than or equal to 4 weeks)

- Able to understand written and spoken English

Exclusion Criteria:

- Under age 18 (children with colorectal cancer)

- Unable to read or understand English

- Vulnerable subjects (except those who are economically or educationally disadvantaged)
We found this trial at
1
site
1 Medical Center Blvd
Winston-Salem, North Carolina 27157
336-716-2011
Wake Forest University Health Sciences Welcome to Wake Forest Baptist Medical Center, a fully integrated...
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Winston-Salem, NC
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