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New treatment option for Cancer Prevention
Official title Eatwell Clinical Trial (R01)
ClinicalTrials.gov ID: NCT07225881
What this study is testing
- What it's testing
- Cancer is a leading cause of death and will affect many people in their lifetimes. Organizations such as the American Cancer Society and the World Cancer Research Fund/American Institute for Cancer Research (WCRF/AICR) have noted that dietary quality is a key factor influencing cancer risk, but most Americans do not meet these dietary guidelines for cancer prevention.
- Which group you join is decided by chance.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 18 and older. Healthy volunteers may be eligible.
You may be able to join if
- Age 18 or older
- Access to technology necessary to receive emails and join videoconferencing meetings
- Ability to read and speak English
- Willingness to be assigned by chance to either study condition, including ability and willingness to attend intervention sessions
- Ability and willingness to attend intervention sessions, receive monthly email messages, and serve in support role if index participant in household...
You likely can't join if
- A medical or psychiatric condition, including self-reported history of anorexia nervosa or bulimia nervosa, that may limit appropriateness of or...
- A psychiatric condition, including self-reported history of anorexia nervosa or bulimia nervosa, that may make it difficult or inappropriate for...
- Currently taking medication that can substantively change appetite or eating behavior, including using of a GLP-1 medication
- Planning to enroll in another lifestyle modification program in the next 18 months
- History of bariatric surgery
- Currently pregnant or planning to become pregnant in the next 18 months
See the full eligibility criteria
- Age 18 or older
- Access to technology necessary to receive emails and join videoconferencing meetings
- Ability to read and speak English
- Willingness to be assigned by chance to either study condition, including ability and willingness to attend intervention sessions
- Ability and willingness to attend intervention sessions, receive monthly email messages, and serve in support role if index participant in household is assigned to Eatwell condition
- Able and willing to visit a commercial laboratory partnered with this project (e.g., Labcorp) in order to have their blood drawn at the time of study visits
- Low adherence to WCRF/AICR's four dietary guidelines (operationalized as a level of intake, based on brief self-report questions administered during phone screening, that corresponds to a score of 2 or less in the...
- Share a household (i.e., a private residence with a shared living space, including kitchen) with an adult who provides informed consent, meets eligibility criteria, and anticipates remaining in this household for the...
- Agree that they will not join another intervention study run by this study team in the next 18 months
- Successful completion by self and household member of all enrollment and baseline data collection tasks
- Have an email that they regularly check and willingness to use that for corresponding to study staff
- Weight at baseline of 396 lbs or less, as the digital scales used for measurement are not able to obtain measurements for weights higher than this
- A medical or psychiatric condition, including self-reported history of anorexia nervosa or bulimia nervosa, that may limit appropriateness of or ability to comply with dietary recommendations
- A psychiatric condition, including self-reported history of anorexia nervosa or bulimia nervosa, that may make it difficult or inappropriate for household member to serve in support role
- Currently taking medication that can substantively change appetite or eating behavior, including using of a GLP-1 medication
- Planning to enroll in another lifestyle modification program in the next 18 months
- History of bariatric surgery
- Currently pregnant or planning to become pregnant in the next 18 months
- Type 1 Diabetes
The study team makes the final eligibility decision.
Where it's taking place
- Philadelphia, Pennsylvania, United States
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 18 years and older. Healthy volunteers may be eligible. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include Philadelphia, Pennsylvania, United States. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.