Efficacy of a Web-based Tailored Self-management Program
Efficacy of a Web-based Self-management Exercise and Diet Intervention Program With Tailored Motivation and Action Planning for Breast Cancer Survivors: A Randomized Controlled Trial
1 other identifier
interventional
59
1 country
4
Brief Summary
Life style interventions that promote exercise and a healthy diet, which have the potential to improve health-related quality of life (HRQOL), may be particularly appropriate for cancer survivors. The previous studies suggested that a key strategy to implement sustainable healthy behavior and improve health was providing appropriate feedback and promoting self-efficacy. Web-based program enables to provide the feedback in a timely manner on a daily basis, to continue the healthy behaviors. Therefore, the investigators developed a web-based, stage-matched Exercise and Diet Planning program, and whether the program can promote significantly greater changes in behavioral outcomes \[goal of exercise (energy expenditure of aerobic exercise ≥ 12.5 kcal/kg/week) and diet (intake of vegetables ≥ 5 serv/day and intake of fruit ≥ 1 serv/day)\], stage of changes for exercise and diet, psychosocial outcomes (HRQOL, fatigue, anxiety and depression) and self-efficacy in implementing goal of exercise and diet among breast cancer survivors in Korea was examined. Hypotheses were following:
- 1.Survivors of a group participating in a web-based, stage-matched Exercise and Diet Planning program (hereinafter called the 'intervention group') will show a more advanced stage of change for exercise and diet compared to survivors in the control group.
- 2.The intervention group will show a higher proportion of attaining goal of exercise (or higher level of energy expenditure of aerobic exercise) compared to the control group.
- 3.The intervention group will show a higher proportion of attaining goal of diet (or higher level of diet quality) compared to the control group.
- 4.The intervention group will show a better HRQOL level compared to the control group.
- 5.The intervention group will show a better self-efficacy level compared to the control group.
- 6.The intervention group will show a lower fatigue level compared to the control group.
- 7.The intervention group will show less anxiety compared to the control group.
- 8.The intervention group will show less depression compared to the control group.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable breast-cancer
Started Oct 2011
Shorter than P25 for not_applicable breast-cancer
4 active sites
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
October 1, 2011
CompletedFirst Submitted
Initial submission to the registry
January 4, 2012
CompletedFirst Posted
Study publicly available on registry
January 19, 2012
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 1, 2012
CompletedStudy Completion
Last participant's last visit for all outcomes
August 1, 2012
CompletedApril 24, 2014
April 1, 2014
5 months
January 4, 2012
April 23, 2014
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Change from baseline in numbers of goal behaviors at 3 months
The primary outcomes of the study are to achieve goals of healthy behaviors as followed: i) exercising≥12.5kcal/kg/week; ii) eating vegetables≥5serv/day and fruits 1-2 serv/day; iii) healthy weight (18.5kg/m2 ≤ BMI \< 25kg/m2) The primary outcome of the study is the increased number of goal behaviors.
Baseline (pre-treatment) and after 12 weeks of intervention (post-treatment)
Secondary Outcomes (4)
Change from baseline in Stage of Change at 3 months
Baseline, 1month, 2 month, 3 month after starting the intervention
Change from baseline in self-efficacy at 3 months
Baseline, 1month, 2 month, 3 month after starting the intervention
Change from baseline in psychosocial outcomes at 3 months
Baseline, 1month, 2 month, 3 month after starting the intervention
Change from baseline in Diet quality at 3 months
Baseline, 1month, 2 month, 3 month after starting the intervention
Study Arms (2)
Web-based, Stage-matched Exercise and Diet Planning program
EXPERIMENTALThe experimental arm is a group that assigned to use web-based, stage-matched exercise and diet planning program.
Non-tailored booklet on exercise and diet
ACTIVE COMPARATORThe control group is provided a booklet containing same information on exercise and diet as in the experimental group's web-based program, but the information on a booklet is not tailored to participants' stage of motivational readiness for exercise and diet based on the TTM.
Interventions
URL is closed The program is 12-week program, provides tailored information on the exercise and diet based on the stage of motivational readiness of TTM. The program is designed to allow to plan a regular exercise of 12.5 MET per week and to recommend to eat number of portions from six food groups for balanced diet tailored to individual's BMI, ideal body weight, and calories needed per day. The program provide the feedback based on the achievement of goals of the behaviors.
The active control group is provided non-tailored booklet on exercise and diet, whose information is same as web-based program except stage-matching.
Eligibility Criteria
You may qualify if:
- Women aged 20 years and older
- Histologically confirmed stage 0 to III breast cancer who received curative breast cancer surgery within 12 months since completion of primary cancer treatment and 2 years since diagnosis
- Serum platelet ≥ 100,000/mm3
- Serum hemoglobin ≥ 10g/dl
- Not met one or more behavior goals: i) energy expenditure of aerobic exercise ≥ 12.5 kcal/kg/week; ii) intake of vegetables except kimchi ≥ 5 serv/day and intake of fruit 1-2 serv/day; iii) maintenance of healthy weight (18.5 kg/m2 ≤ BMI \< 23 kg/m2)
- Ability to use internet, and being accessible internet at home
- Mobile phone user
- Consent form to participate in the study
You may not qualify if:
- Currently receiving any cancer treatment
- Conditions that could limit adherence to an unsupervised exercise program such as uncontrolled congestive heart failure or angina, recent myocardial infarction, or breathing difficulties requiring oxygen use or hospitalization; walker or wheelchair use; or plans to have hip or knee replacement
- Conditions that could interfere with a high vegetable and fruit diet, such as kidney failure or chronic warfarin use
- Progressive malignant disease or additional primary cancers
- Infectious condition (body temperature ≥ 37.2℃ or WBC ≥ 11,000mm3)
- Inability to use computer or internet
- Visual and motor dysfunction
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- National Cancer Center, Korealead
- Seoul National Universitycollaborator
- Asan Medical Centercollaborator
- Korea University Anam Hospitalcollaborator
Study Sites (4)
National Cancer Center
Gyenggi-do, Goyang-si, 410-769, South Korea
Asan Medical Center
Seoul, South Korea
Korea University Anam Hospital
Seoul, South Korea
Seoul National University
Seoul, South Korea
Related Publications (1)
Lee MK, Yun YH, Park HA, Lee ES, Jung KH, Noh DY. A Web-based self-management exercise and diet intervention for breast cancer survivors: pilot randomized controlled trial. Int J Nurs Stud. 2014 Dec;51(12):1557-67. doi: 10.1016/j.ijnurstu.2014.04.012. Epub 2014 May 1.
PMID: 24856854DERIVED
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
YoungSung Lee, PhD
National Cancer Center
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- SUPPORTIVE CARE
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER GOV
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Head
Study Record Dates
First Submitted
January 4, 2012
First Posted
January 19, 2012
Study Start
October 1, 2011
Primary Completion
March 1, 2012
Study Completion
August 1, 2012
Last Updated
April 24, 2014
Record last verified: 2014-04