- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04919759
Feasibility of Technology Mediated Lifestyle Intervention for Overweight and Obese Young Adults (Rashakaty)
June 3, 2021 updated by: Habiba I. Ali, United Arab Emirates University
Development, Implementation and Evaluation of Technology Mediated Lifestyle Intervention for Promoting Weight Loss and Improving Nutrition Behaviors Among Young Adults
Rashakaty (Fitness for Me) study aimed to design a new technologies-based intervention using a website and smart phone applications and to test the feasibility of implementing a lifestyle intervention using these technologies for overweight and obese university students.
The intervention was implemented in two universities in the United Arab Emirates
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Detailed Description
Poor eating habits and sedentary lifestyle are common among young adults and increase risk for chronic diseases in subsequent years of life.
Rashakaty (Fitness for Me) study aimed to design a new technologies-based intervention using a website and smart phone applications and to test the feasibility of implementing a lifestyle intervention using these technologies for overweight and obese university students.
The study intervention was guided by Social Cognitive Theory.
The study involved the development of a website, integrating educational material and mobile applications for monitoring diet and physical activity and a16-week feasibility trial to promote weight loss, improve food choices and increase physical activity levels.
The trial consisted of two arms: Rashakaty Basic (R-Basic) and Rashakaty Enhanced (R-Enhanced).
Study Type
Interventional
Enrollment (Actual)
246
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
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Select State Or Region
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Al Ain, Select State Or Region, United Arab Emirates
- United Arab Emirates University
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-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
18 years to 35 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Female
Description
Inclusion Criteria:
- Overweight or obese (BMI ≥25.0
- Adults: Female
- Age: 18-35 years
- Current user of a smart phone
- Student in one of the two target universities in the United Arab Emirates
- Living in or off the university campus
Exclusion Criteria:
- Past or planned weight loss surgery
- Pregnant or breastfeeding
- Lost 7 kg in the past 3 months
- Following any weight loss program for 3 months or more
- Taking any steroid or thyroid hormones treatment or any other medication that may affect body weight
- Enrolled in medical and nutrition programs since one of the program components was nutrition knowledge assessments
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Non-Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
Active Comparator: Rashakaty Basic (R-Basic)
Participants in the R-Basic intervention arm had access to a website that contained the study questionnaires and nutrition education materials
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Participants in the R-Basic arm received access to a static website that contained educational materials on healthier eating and physical activity and the study questionnaires.
The R-Basic intervention was implemented in the University of Sharjah.
Other Names:
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Experimental: Rashakaty Enhanced (R-Enhanced)
Participants in the R-Enhanced intervention were given access to smart phones applications for monitoring diet and physical activity levels as well as an online access to a nutritionist
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The R-Enhanced intervention was guided by the Social Cognitive Theory and employed a variety of behavior modification strategies, including self-monitoring, goal setting, self-efficacy, and social support to facilitate changes in diet and physical activity.
In addition, participants in the R-Enhanced intervention had online access to a nutritionist.
The R-Enhanced intervention was implemented in the United Arab Emirates University.
Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Body weight
Time Frame: 16 weeks
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changes in body weight
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16 weeks
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Body composition
Time Frame: 16 weeks
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Changes in body composition (percent body fat)
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16 weeks
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Nutrition knowledge
Time Frame: 16 weeks
|
The General Nutrition Awareness Questionnaire (GNKQ) validated by Parmenter and Wardle in the UK. was used after local adaptation.
Four main categories containing a total of 58 items were assessed:1) Awareness of dietary recommendations (11 items); 2) Knowledge of sources of nutrients (37 items); (3) Using the information to make dietary choices (5 items); and 4) Awareness of diet-disease relationships (5 items).
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16 weeks
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Physical activity
Time Frame: 16 weeks
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Changes in physical activity (number of days and duration) was used using The International Physical Activity Questionnaire (IPAQ) - Short Form
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16 weeks
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Perceived social support from family and closest friends.
Time Frame: 16 weeks
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Perceived social support for healthier foods and physical activity scale of Health Beliefs Questionnaire which was originally developed by Anderson, E. and colleagues was used after adaptation for university students in the UAE.
The social support subscale (16 items for healthy eating and 7 items for physical activity) measures social influences on participants by their family members and closest friends.
Each question is scored 1-5 (1 - Strongly disagree, 5 - Strongly agree).
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16 weeks
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Perceived self-efficacy for healthier eating and physical activity
Time Frame: 16 weeks
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Perceived self-efficacy scale of Health Beliefs Questionnaire which was originally developed by Anderson, E. and colleagues after local adaptation was used.
It consists of 33 items for healthy eating and 24 items for physical activity.
The healthy food efficacy measure assesses the respondent's confidence in reducing fat, reducing sugar consumption and increasing fruit and vegetable intake.
The physical activity measure consists of two subscales: overcoming barriers to engaging in physical activity and integrating physical activity into the daily routine.
Each question is scored 0 to 100 (certain I cannot) to 100) all or most of the time.
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16 weeks
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Habiba I Ali, PhD, RD, CDE, United Arab Emirates University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
August 21, 2016
Primary Completion (Actual)
May 31, 2017
Study Completion (Actual)
May 31, 2017
Study Registration Dates
First Submitted
May 30, 2021
First Submitted That Met QC Criteria
June 3, 2021
First Posted (Actual)
June 9, 2021
Study Record Updates
Last Update Posted (Actual)
June 9, 2021
Last Update Submitted That Met QC Criteria
June 3, 2021
Last Verified
June 1, 2021
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 33/2014/2015
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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