Closed for Recruitment
Study / Trial Background
The purpose of the study is to learn how to make homes more supportive of healthy eating and physical activity. As part of the study, participants will be randomly assigned to one of two groups. One group will receive materials with information on healthy eating and physical activity. The materials will be mailed 3 times over a 5 month period. The other group will work with a coach to make their homes more supportive of healthy eating and physical activity. Working with a coach involves 3 home visits and 4 coaching telephone calls over a 5 month period. This group will also receive materials by mail 4 different times. All participants will be asked to complete 7 telephone interviews over a 1 year period. Participants will also be asked to wear an accelerometer, a small portable device that tracks movement from physical activity, for 7 days at 2 different points in the study.
Results from the National Survey of Lead and Allergens in Housing suggest that the construction and operation of a house might have a significant influence on the level of allergens. For example, the strongest predictors for dust mite allergen were indoor humidity and age of the home.
In collaboration with researchers at Advanced Energy, a non-profit company that designs and builds energy-efficient components for homes, we have designed and implemented a study that is investigating whether construction techniques can effect levels of indoor allergens and air pollutants.
Being tested is a construction system known as SystemVision Plus which was developed by the building science team at Advanced Energy.
This system was designed to reduce relative humidity, improve temperature control, and reduce particles in indoor air.
This study examines whether we can detect a difference in the environments of the 16 control houses and 20 intervention houses over the course of 18 months. The follow-up of homes will be completed in June of 2006.
The following indicators will be monitored to determine differences between the intervention and non-intervention homes:
- Relative Humidity
- Allergens (endotoxin, mold spore, dust mites, etc.)
- Volatile organic compounds
For more information on this study, please visit the Clinical Trials webpage for this study.
The study has completed enrollment.
- Ages Eligible for Study: 35 Years to 65 Years
- Genders Eligible for Study: Female
- Accepts Healthy Volunteers: Yes
- 35-65 years old
- BMI greater than or equal to 25
- Speak English
- Must live with at least one other person
- Live within 30 miles of 1 of 9 clinics referring patients in the study
- Must have no contraindications for physical activity
- Must have no contraindications for participating in a medically unsupervised study
- 1 person per household
What will you do?
Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study.
What will NIEHS do?
Primary Outcome Measures:
- Diet & Physical Activity [ Time Frame: Baseline, 6 months, and 12 months ]
[ Designated as safety issue: No ]
- Diet and physical activity will be assessed by telephone interviews. Physical activity will also be assessed using accelerometers at baseline and 6 months.
Secondary Outcome Measures:
- Weight [ Time Frame: Baseline, 6 months, and 12 months ] [ Designated as safety issue: No ]
Self-report weight will be assessed by telephone interview.
- Changes in the home physical and social environment [ Time Frame: Baseline, 6 months, and 12 months ] [ Designated as safety issue: No ]
A home environment survey will be administered by telephone.
Study / Trial Location
Centers for Disease Control and Prevention
Southwest Georgia Cancer Coalition
Protocol Number: HHHF