N/A N=615 Randomized Double-blind Prevention

Individual Counseling and/or Computer-Based Counseling in Helping Healthy Women Adopt a Cancer Prevention Diet

Unspecified Adult Solid Tumor, Protocol Specific

Bottom Line

View on ClinicalTrials.gov: NCT00217490 ↗

Enrolled (actual)

615

Serious AEs

0.0%

Results posted

Apr 2017

Primary outcome: Primary: Change in Fruit, Vegetable Consumption as Measured by Food Frequency Questionnaire at 3 Months — 2.7272727; 2.9758065; 2.7330645; 0.4720000 number of servings per day

Study Design & Population

Study type: Interventional
Phase: N/A
Interventions: dietary counseling via computer (Behavioral); dietary counseling via nutritionist (Behavioral); combined computer and nutritionist (Behavioral); physical activity counseling via computer (Other)
Age: Adult, Older Adult · 30+ yrs
Sex: Female
Sponsor: Kaiser Permanente
Primary completion: Sep 2008

Outcome Measures

Outcome	Result	p-value
PRIMARY Change in Fruit, Vegetable Consumption as Measured by Food Frequency Questionnaire at 3 Months	2.7272727; 2.9758065; 2.7330645; 0.4720000	—
PRIMARY Change in Percentage of Fat Consumed	-4.653333; -5.3439516; -6.0113710; -1.4154400	—

Summary

RATIONALE: Eating a diet high in fruits and vegetables and low in fat may lower the risk of some types of cancer. Dietary counseling may be effective in helping women change to a healthy diet. PURPOSE: This randomized clinical trial is studying how well individual counseling and/or computer-based counseling work in helping healthy women adopt a cancer prevention diet.

Eligibility Criteria

DISEASE CHARACTERISTICS:

Healthy participant
Not undergoing care for cancer
Kaiser Permanente health plan member for at least 2 years
No current dietary goals
No diet comprising an average consumption of > 4 combined servings of fruits and vegetables per day and/or fat consumption below 30% of total energy
No physician-prescribed diets

PATIENT CHARACTERISTICS:

Age

30 to 70

Sex

Female

Performance status

Not specified

Life expectancy

Not specified

Hematopoietic

Not specified

Hepatic

Not specified

Renal

Not specified

Other

Not pregnant

PRIOR CONCURRENT THERAPY:

Biologic therapy

Not specified

Chemotherapy

Not specified

Endocrine therapy

Not specified

Radiotherapy

Not specified

Surgery

Not specified

View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT00217490). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.