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Spots Global Cancer Trial Database for The Inland Northwest Colon Cancer Survivor's Study

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Trial Identification

Brief Title: The Inland Northwest Colon Cancer Survivor's Study

Official Title: Self Reported Changes in Quality of Life, Demands of Illness, and Sexual Function in Colon Cancer Survivors.

Study ID: NCT01775254

Conditions

Colon Cancer

Interventions

Study Description

Brief Summary: The overall purpose of this study was to address the following questions by describing the trajectory of early survivorship in individuals who undergo both surgical and medical management of colon cancer. What are the changes in quality of life, demands of illness, sexual function, and peripheral neuropathy, following curative resection during the first year of treatment and recovery? Is there an interaction between exposures to chemotherapy and changes over time in these outcomes?

Detailed Description: The population of interest included colon cancer survivors of both sexes, 18 to 90 years of age, who underwent one of two types of surgical resection and who may receive adjuvant chemotherapy. The prospective design with two cohorts representing exposure to chemotherapy (chemotherapy vs. no-chemotherapy) described the changes in quality of life, demands of illness, sexual function, and peripheral neuropathy, which occurred following curative resection. An analysis of the interaction between time (four measurement occasions) and the independent variable of chemotherapy group by mean values of quality of life, sexual function, peripheral neuropathy, and demands of illness addressed the central thesis question. Specific Aims 1. Examine the relationships among quality of life, demands of illness, sexual functioning, and peripheral neuropathy, for the total sample and by chemotherapy group. 2. Examine changes within-subjects (four measurement occasions), between-group (chemotherapy, no-chemotherapy) differences, and the interaction between time and chemotherapy group for quality of life, demands of illness, sexual functioning, and peripheral neuropathy across four measurement occasions.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Deaconess Hospital, Spokane, Washington, United States

Sacred Heart Medical Center, Spokane, Washington, United States

Holy Family Hospital, Spokane, Washington, United States

Valley Hospital, Spokane, Washington, United States

Contact Details

Name: Jeanne M Robison, PhD, ARNP

Affiliation: Washington State University, College of Nursing

Role: PRINCIPAL_INVESTIGATOR

Name: Mel Haberman, PhD, FAAN

Affiliation: Washington State University, College of Nursing

Role: PRINCIPAL_INVESTIGATOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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