N/A
Completed N=26
Feasibility of a Campaign Intervention Compared to a Standard Behavioral Weight Loss Intervention in Overweight and Obese Adults
Source: ClinicalTrials.gov NCT01803737 ↗Enrolled (actual)
26
Serious AEs
0.0%
Results posted
Feb 2014
Primary outcomePrimary: Change in Body Weight — -5.6; -3.1 kg
Summary
The purpose of this study is to examine the feasibility of a campaign intervention for weight management compared to a standard behavioral weight loss intervention in overweight and obese adults.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Change in Body Weight |
-5.6; -3.1 | — |
| SECONDARY Change in Physical Activity |
983.3; 776.3 | — |
| SECONDARY Change in Dietary Intake: Kcals/Day |
474.8; 242.5 | — |
| SECONDARY Change in Dietary Intake: % Fat |
-3.26; -0.00 | — |
| SECONDARY Change in Dietary Intake: % Protein |
0.73; 0.44 | — |
| SECONDARY Change in Dietary Intake: % Carbohydrate |
0.64; 0.90 | — |
| SECONDARY Completion of Self-monitoring of Dietary Intake and Physical Activity |
91.6; 60.1 | — |
| SECONDARY Change in Weight Loss Self-efficacy |
28.3; 16.3 | — |
| SECONDARY Autonomous and Controlled Motivation |
6.3; 5.3; 2.9; 2.9 | — |
Eligibility Criteria
Inclusion Criteria
- 18-55 years of age
- Body mass index (BMI) ranging from ≥25.0 kg/m² to 45.0 kg/m²
- Ability to provide informed consent
Exclusion Criteria
- Regular exercise participation of at least 20 minutes per day on at least 3 days per week during the previous six months.
- Participation in a previous physical activity or weight management research project in the previous 6 months.
- Weight loss of ≥5% of current body weight in the previous 6 months.
- For women, those currently pregnant, pregnant during the previous 6 months, or plan on becoming pregnant in the next 6 months.
- History of myocardial infarction, coronary bypass surgery, angioplasty, or other heart-related surgeries.
- History of orthopedic or physical complications that would prevent participation in exercise.
- Currently taking any prescription medication that may affect metabolism and/or body weight (e.g., synthroid).
- Currently being treated for any condition that could affect body weight, such as coronary heart disease, diabetes mellitus, uncontrolled hypertension, cancer, depression, and anxiety.
- Currently being treated for any psychological issues or problems, taking any psychotropic medications, or receiving treatment with psychotropic medications within the previous 6 months.
- Resting systolic blood pressure ≥150mmHg or diastolic blood pressure ≥100mmHg. Subjects with controlled hypertension will be allowed to participate if they obtain a medical doctor's written consent to ensure that it is safe to participate in a weight loss intervention.
- Currently do not have access to a computer and the Internet.
Data sourced from ClinicalTrials.gov (NCT01803737). 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. Informational only — not medical advice.