Pounds Off Digitally Study: A Podcasting Weight Loss Intervention (POD)
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Purpose
Participants in both the existing and enhanced podcast groups will lose weight. The enhanced podcasting group will have a greater increase in weight loss, elaboration, self-efficacy, and perceived control than the existing podcast group.
| Condition | Intervention | Phase |
|---|---|---|
|
Weight Loss |
Behavioral: podcasting |
Phase 1 |
| Study Type: | Interventional |
| Study Design: | Intervention Model: Parallel Assignment Masking: Open Label Primary Purpose: Treatment |
| Official Title: | Pounds Off Digitally Study: A Podcasting Weight Loss Intervention |
- weight [ Time Frame: 12 weeks ] [ Designated as safety issue: No ]
- elaboration [ Time Frame: 12 weeks ] [ Designated as safety issue: No ]
| Enrollment: | 94 |
| Study Start Date: | January 2008 |
| Study Completion Date: | June 2008 |
| Primary Completion Date: | May 2008 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
| Active Comparator: Control (available) podcast | Behavioral: podcasting |
| Experimental: Enhanced podcast | Behavioral: podcasting |
Detailed Description:
We will conduct a weight loss intervention study among adults. Using the weight loss podcast that receives the highest rating from a previous content analysis, we will conduct an intervention comparing the best existing weight loss podcast to an enhanced podcast. The enhanced podcast will be based on theoretical constructs that have been shown to be effective in producing weight loss in other research studies. We will then evaluate the effectiveness of podcasting to promote weight loss in adults. Weight change from baseline to 12-weeks and changes in psychosocial measures will be used to assess differences between the existing podcast, enhanced podcast, and control conditions. In conclusion, this research study aims to find innovative and inexpensive ways to help people lose weight. Podcasting has the possibility of reaching a wide range of age and ethnic groups and will allow people to receive weight loss information when and where it is convenient for them.
Eligibility| Ages Eligible for Study: | 18 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
be 18-50 years old be overweight or obese (BMI between 25-35) but not severely or morbidly obese live in the Chapel Hill area be able to attend an introduction meeting and weigh-in before the study and a weigh-in after the study have access to the Internet and a computer with a sound card have a working MP3 player that can connect to a computer have access to a scale be willing to be randomized to any group
Exclusion Criteria:
smoker current major health or psychiatric diseases, drug or alcohol dependency, uncontrolled thyroid conditions, eating disorder, or pregnancy participation in a weight loss program or taking weight loss medications
Contacts and Locations| United States, North Carolina | |
| UNC-Chapel Hill | |
| Chapel Hill, North Carolina, United States, 27514 | |
More Information
No publications provided by University of North Carolina, Chapel Hill
Additional publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
| Responsible Party: | Gabrielle Turner-McGrievy, UNC-Chapel Hill |
| ClinicalTrials.gov Identifier: | NCT00771095 History of Changes |
| Other Study ID Numbers: | 07-0430-03 |
| Study First Received: | October 9, 2008 |
| Last Updated: | October 9, 2008 |
| Health Authority: | United States: Institutional Review Board |
Keywords provided by University of North Carolina, Chapel Hill:
|
weight loss elaboration self efficacy |
Additional relevant MeSH terms:
|
Weight Loss Body Weight Changes Body Weight Signs and Symptoms |
ClinicalTrials.gov processed this record on May 19, 2013