Prepare - How to Reach Women of Reproductive Age With Obesity to Support Weight Loss Before Pregnancy?

Sponsor
Harvard Pilgrim Health Care (Other)
Overall Status
Completed
CT.gov ID
NCT03663621
Collaborator
Massachusetts General Hospital (Other)
99
1
28.6
3.5

Study Details

Study Description

Brief Summary

Researchers at Harvard Pilgrim Health Care Institute and Massachusetts General Hospital are conducting a study to learn more about how best to reach out to women (age 18-45) who are thinking about a pregnancy in the next couple of years and currently have a BMI greater than 30 kg/m2.

Interested participants will be asked to complete a 15-minute survey. The survey will ask some more questions about their prior reproductive health history, opinions and experiences regarding lifestyle, weight and health. After completing the survey, researchers would like to arrange a time to complete a 20- to 30-minute semi-structured interview about their perceived health in the process of planning pregnancy.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    The purpose of this study is to learn the best ways to support healthful behaviors and weight loss prior to pregnancy. Researchers are also interested in what motivates or prevents women of reproductive age from engaging in a structured weight loss program. Participants will be asked for no more than an hour of their time to complete a brief survey and participate in an interview. This study is being conducted by Harvard Pilgrim Health Care Institute. This study is being paid for by the Nutrition Obesity Research Center at Harvard (NORCH).

    At the end of the interview, study staff will also talk to participants about the opportunity to be referred to the Mass General Weight Center if they are interested in participating in a program now being offered there.

    If participants elect to participate in a program at the weight center, researchers would then like to complete 2 more short interviews with these participants about that process. The first will be about 5 minutes and will take place just after the initial Weight Center Orientation, and the last will be about 10 minutes and take place after 3 months of participation. During this final interview, researchers will ask for participant opinions about the program that they have just participated in.

    Study Design

    Study Type:
    Observational
    Actual Enrollment :
    99 participants
    Observational Model:
    Cohort
    Time Perspective:
    Prospective
    Official Title:
    How to Reach Women of Reproductive Age With Obesity to Support Weight Loss Before Pregnancy?
    Actual Study Start Date :
    Jan 25, 2018
    Actual Primary Completion Date :
    Aug 31, 2019
    Actual Study Completion Date :
    Jun 15, 2020

    Arms and Interventions

    Arm Intervention/Treatment
    Initial survey and interview (Aim 2)

    Participants in Aim 2 will be asked to complete an initial 15-minute survey and 20-30 minute semi-structured interview. The purpose of this study is to learn the best ways to support healthful behaviors and weight loss prior to pregnancy. Researchers are also interested in what motivates or prevents women of reproductive age from engaging in a structured weight loss program.

    Formal weight loss program (Aim 3)

    Participants in Aim 3 have expressed interest in referral to the Mass General Weight Center. The purpose of this study is to learn what motivates or prevents women of reproductive age from engaging in a structured weight loss program. Researchers will ask for no more than a half hour of participant's time to complete a 5- minute interview following Orientation at the Weight Center and another 10-minute interview after a participant has participated in a program offered at the Weight Center.

    Outcome Measures

    Primary Outcome Measures

    1. Participant recruitment feasibility [1 year]

      Feasibility determined by compiling the actual number of participants recruited divided by the time and resources necessary to achieve that number participants for each recruitment strategy.

    Secondary Outcome Measures

    1. Participants' attitudes and perceptions of their own health risks with regard to weight-related complications [1 year]

      Participants are asked to measure levels of agreement/disagreement with their perceived health risk for ten weight related complications as follows: developing developing diabetes, developing cancer, developing heart disease, developing high blood pressure, developing high cholesterol, being able to get pregnant, having diabetes during pregnancy, having high blood pressure during pregnancy, having a large baby, and having to undergo a c-section

    2. Participant adherence during a structured weight loss program. [1 year]

      Participants' attendance is recorded throughout the duration of a 12-week weight loss program. Successful adherents will have attended >70% of meetings.

    3. Participants' estimated time frame before trying to get pregnant and willingness to delay their pregnancy attempt in order to complete a structured weight loss program. [1 year]

      Participants are interviewed to assess their current time frame before actively trying to get pregnant. Participants are also asked if they are willing to delay a pregnancy attempt and if so, for how long.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 45 Years
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Women aged 18-45 years old,

    • BMI>30 mg/m2,

    • thinking about planning a pregnancy in the next 2 years

    Exclusion Criteria:
    • Previous bariatric surgery,

    • currently pregnant

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Harvard Pilgrim Health Care Institute Boston Massachusetts United States 02215

    Sponsors and Collaborators

    • Harvard Pilgrim Health Care
    • Massachusetts General Hospital

    Investigators

    • Principal Investigator: Marie-France Hivert, MD, MMSc, Harvard Pilgrim Health Care Institute

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Harvard Pilgrim Health Care
    ClinicalTrials.gov Identifier:
    NCT03663621
    Other Study ID Numbers:
    • 1105007
    First Posted:
    Sep 10, 2018
    Last Update Posted:
    Jul 30, 2020
    Last Verified:
    Jun 1, 2020
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jul 30, 2020