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Completed

NCT Number: NCT00561977

Cancer Dietary Objectives Study

We hypothesize that adding beneficial high fiber foods to the diet will result in better overall dietary quality (measured by the Alternate Healthy Eating Index), which has been shown to be associated with cancer, than either reducing saturated fat, or a combination of high fiber and low saturated fat.

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Key information

Age range

21 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

UMass Medical School

Worcester, Massachusetts, 01655, United States

About this study

Summary of Grant:

Several studies have demonstrated that poor dietary quality is associated with obesity and certain cancers, such as gastrointestinal, colorectal, and hormonal cancers. Dietary interventions aimed at improving diet are plagued by poor adherence, possibly due to the complexity of changing multiple diet components. Complex public health messages are associated with worse adherence and reduced capacity to impact health outcomes. If a simple public health recommendation for diet was effective at changing multiple aspects of diet, adherence and impact could be maximized. However, research has yet to test which single dietary message has the greatest impact on overall diet quality, and consequently, potential for cancer and heart disease prevention. Thus far, dietary interventions have tested varying combinations of multiple recommendations; however, a single dietary recommendation may have a synergistic beneficial effect on other areas of diet, precluding the need to make the message overly complex.

The present study compares 3 dietary change conditions that are hypothesized to have high potential for synergistic effects on other unaddressed areas of diet, and consequently overall dietary quality. Patients were randomized to one of three arms:

  • low saturated fat diet (≤7% of total calories);
  • high fiber diet (≥30 grams of total fiber per day);
  • combination arm: low saturated fat and high fiber.

Each participant was instructed to reduce calories by -500 kcal/day from his/her resting metabolic rate (RMR), but total calories was not less than 1200 calories per day.

Additionally, Dr. Ira Ockene, professor of medicine, director of preventive cardiology program, generously offered to pay for blood draws and blood lipids and glucose analysis at each visit to make the study valuable from both cancer and heart disease research perspectives.

Specific aims:

  • Develop intervention materials. Intervention materials that specifically aid participants towards a low saturated fat or high fiber diet, or combination change developed for each condition.
  • Preliminary test of intervention. We will calculate change in diet quality, lipids, body weight, waist circumference, and blood pressure at 3- and 6-months. We hypothesize that the single change conditions will produce more changes than the complex condition and that adding beneficial high fiber foods to the diet will result in improved dietary quality (measured by the Alternative Healthy Eating Index) than reducing saturated fat. Secondary outcomes include calorie intake, micro- and macronutrients at baseline, physical activity, and observe changes at 3- and 6-months.
  • Adherence. We will examine adherence to the treatment protocol so that appropriate adjustments to the intervention can be made, if necessary, to enhance adherence in the larger randomized clinical trial.
  • Data for sample size estimation. We will document means and standard deviations on measures so that sample size can be estimated for the larger randomized clinical trial.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • BMI ≥25, and ≤40.
  • >=21 years of age, less than 81 years of age.
  • has primary care physician's approval to participate in all aspects of the study,
  • speaks, reads, and understands English at 6th grade level minimum
  • residing in local area for the duration of the study.
  • available for bi-monthly sessions (6 individual nutrition counseling visits)

Exclusion criteria

  • presence of a psychological disorder that will limit his/her ability to participate (such as an eating disorder, uncontrolled bipolar disorder)
  • unwilling to provide informed consent
  • presence of unstable medical disorder (e.g., uncontrolled hypertension, uncontrolled diabetes, etc), or a medical disorder associated with a life expectancy less than 2 years.
  • currently taking any medication known to affect weight or appetite
  • smokes more than 3 cigarettes a day on average
  • Has a dietary restriction that precludes changing to the healthy diet, i.e.; Crohn's disease, ulcerative colitis, renal disease, active diverticulitis, etc.
  • currently following a specific diet plan (low saturated fat/meat, or high fiber)
  • does not have a telephone
  • Pregnant, or planning to become pregnant (participant will be asked this question in telephone screening. If the participant becomes pregnant, they are asked to inform the principal investigator)
  • Has an active drug or alcohol problem within the past year -

Treatment and study plan

High fiber diet

Behavioral

high fiber diet (≥30 grams of total fiber per day); reduction of calories to -500 from resting metabolic rate (RMR), not less than 1200 kcal per day.

low saturated fat diet

Behavioral

low saturated fat diet (≤7% of total calories); -500 calories from RMR, not less than 1200 kcal/day.

Combination diet

Behavioral

combination low saturated fat high fiber diet, with calorie restriction as specified.

Primary outcomes

  1. Dietary Quality

    Time frame: 6 mos

    Dietary quality was measured by the Alternative Healthy Eating Index (AHEI), a scale of healthy eating that goes from zero to 80 (best score).

  2. Dietary Quality, Possible Score From Zero to 80 (Best Quality Diet).

    Time frame: 3 months

    The AHEI consists of 8 components (eg, vegetables,trans fat). Each contributed 0-10 points to the total score; a score of 10 indicates that the recommendations were fully met, whereas a score of 0 represents the least healthy dietary behavior. Intermediate intakes were scored proportionately between 0 and 10. All component scores were summed to obtain a total AHEI score ranging from zero(worst) to 80(best).

Secondary outcomes

  1. Change in Weight From Baseline to 3 Months

    Time frame: 3 months

  2. Change in Weight From Baseline to 6 Months

    Time frame: 6 months

  3. Change in Calories From Baseline to 3 Months

    Time frame: 3 months

    kilocalories

  4. Change in Calories From Baseline to 6 Months

    Time frame: 6 months

    kilocalories

Sponsors and collaborators

Lead sponsor

University of Massachusetts, Worcester

Other

Collaborators

  • American Cancer Society, Inc.

Registry information

Official study title

Finding a Simple Message to Improve Dietary Quality for Cancer and Heart Disease

Acronym: CanDo

Important dates

Study start
2007
Primary completion
2008
Study completion
2009
First posted
Nov 21, 2007
Registry last updated
Sep 2, 2011

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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