OverweightSMARTERNCT02829632
Feasibility Study of Receiving Feedback Messages Based on Self-monitored Dietary Intake
A study testing Group Sessions, Feedback and Self-monitoring in people with Overweight and Obesity, run by University of Pittsburgh at 1 site in United States.
Trial summary
Brief Summary: This randomized clinical pilot will test the feasibility of having individuals self-monitor for 12 weeks and based on what the participants record be given feedback messages. The investigator will use this information to refine the questions and data collection procedures for the larger study. Read more about this study
- Who is it for?
- Ages 18 years and olderHealthy volunteers can take part
- Conditions the study is for
- Overweight, Obesity
- What is being tested?
- Group Sessions, Feedback and Self-monitoring
- Type of treatment
- Lifestyle or therapy programme
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 39 participants
- Where
- 1 siteUnited States
- Study dates
- Mar 2015to Jun 2015
- Phase
- Interventional
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Who may be able to join
- age 18 years or older
- BMI between 27-43
- have an Android smartphone,
- has not used app for self-monitoring at least 4 days/week for the past 3 months
- can attend group meetings.
Who cannot join
- persons who plan to become pregnant
- have diabetes or a medical condition in which weight loss in contraindicated
- unable to walk for exercise
- on a weight loss drug
- had bariatric surgery
- plans to relocate within 3 months of recruitment
- currently in a weight loss program. -
Trial locations and contacts
1 site in 1 country.
United States1 site
University of Pittsburgh
Pittsburgh, Pennsylvania, 15261
About this study
Official title: 12 Weeks Weight Loss Study Using Feedback Messages Delivered Via Smartphone
Brief Summary: This randomized clinical pilot will test the feasibility of having individuals self-monitor for 12 weeks and based on what the participants record be given feedback messages. The investigator will use this information to refine the questions and data collection procedures for the larger study.
Participants will be randomized into 3 groups
Read more
- self-monitoring only
- self-monitoring w/ feedback messages
- self-monitoring w/feedback messages and group sessions Feedback messages will be delivered up to 4 times per day using a different schedule. The group sessions will be held in the 2nd, 4th and 8th week of the 12-week study.
All participants will be asked to complete questionnaires and 2 assessment visits at baseline and 12 weeks.
Read the detailed description
Research Strategy. The investigator will randomize 45 overweight/obese adults to one of 3 groups: (1) Control (Con) - no FB, no Behavioral Lifestyle Program (BLP), (2) FB Only, no BLP, and (3) FB+BLP. All subjects will use a smartphone to self-monitor diet and PA. The subjects will download a feedback system onto the Android operating system smartphone that was developed for this study called the SMARTER. The algorithm was developed by Dr. Lora Burke of the University of Pittsburgh. All groups will attend a one-time how to self-monitor using the smartphone session and receive education materials at baseline. The FB Only and FB+BLP groups will receive up to 4 daily FB messages, based on progress in attaining target behavior. The FB will be delivered on a variable ratio schedule and tailored to data in subjects' recordings. FB+BLP participants will receive a face-to-face BLP intervention that will include 3 group sessions over 12 weeks. Also to not confound the effect of the daily FB, the interventionists will not provide feedback to the weekly diaries. Sample. The investigator will recruit from the community 45 adults, over the age of 18. All participants need to be randomized prior to the beginning of the 3 BLP sessions since the sessions are conducted as a closed group. The randomization scheme will be implemented via a computerized program (Visual Basic 6.0) using minimization method. The randomization will be overseen by a statistician (Co-I: S Sereika). Each of the 3 conditions will be assigned a total of 15 subjects with randomization stratified by gender and ethnicity/race. Intervention. Those in the Con and FB Only groups will receive a 1-hr session on provided calorie prescription for weight loss and self-monitoring and associated education materials. Only those in FB+BLP will receive a 3-session BLP for a healthful lifestyle and weight loss. The groups will meet in the School of Nursing and will be led by a trained interventionist. Protocol for Self-monitoring: All participants will be subscribed to LoseIt!, an online self-monitoring service that can be accessed via the smartphone and computer. This will be used in place of the traditional paper diary. This software permits self-monitoring of diet, PA, and weight; it also provides feedback on up to 9 macronutrients based on a database of 60,000 foods. Because of the investigator's ongoing working relationship with the developers of LoseIt! program, the investigator will have access to LoseIt! Connect, a custom portal created by LoseIt! for centralized user management. This permits the investigators to view participants' entries and set custom controls on participants use, (e.g., disabling particpants' ability to share data with outsiders). All participants will be encouraged to self-monitor diet and self-report weight. Participants who do not have scales will be given one for the duration of the study and be ask to return it at the completion of the study. Participants see the nutrient value of each food and the calculated subtotals. The interventionists will have access to the diaries so participants can contact a participant if there is any concern about the reported eating behaviors. This is the same procedure used for the past 4 years in the EMPOWER Study (IRB - PRO10100504). At the training session, participants will be advised on how to change the privacy settings on Lose It!. General Information about Feedback Algorithm. The FB algorithm programmed in the FB app will use real-time synced self- monitoring data to send messages that are responsive to the participants' entries. The server will deliver a message that will be displayed on the screen of the smartphones so the person does not need to make extra clicks to view it. The FB messages will address one target behavior at a time, e.g., self-monitoring or calorie intake. At the baseline education session for the FB Only group or the first BLP session for FB+BLP, the individual will make a diary entry; the system will send a FB message shortly thereafter to provide immediate reinforcement for self-monitoring. Then the FB will be delivered on the incremental 1-4 x/d schedule, contingent on progress in self-monitoring and in attaining the person's daily calorie goal. Rules will be applied to the delivery of messages to FB Only and FB+BLP, e.g., messages will be delivered between the hours set by the participants on particpants phone, e.g., 8 AM and 9:30 PM, and content will be guided by the parameters built into the algorithm. In the implementation of the proposed FB intervention, the investigators will exercise caution and sensitivity regarding participants' reception of the messages. In the SMART Trial, the messages were motivating and reinforcing, not noting deficiencies in behavior or progress not made; however, the messages will provide guidance for corrective action when the person is not following the behavior that would be consistent with the pre-established goals. Space does not permit extensive message samples but examples might be as follows. Excellent job on increasing fruits in your diet. OR Super job staying within the fat limits. Go easy on high fat foods tonight; consider having a big salad with nonfat dressing. Protocol for the Behavioral Lifestyle Program (BLP) intervention: Group Sessions: Participants will receive nutritional and behavioral counseling; practical hands-on experiences to develop skills to implement a healthy lifestyle (e.g., practice mindful eating, portion size, modify foods or meals to reduce fat content) in three 1 hour group sessions. The groups will meet evenings and will be led by the multidisciplinary team (behavioral scientists, nutritionists that has been trained by the PI and Co-I (Burke and Ewing). The group sessions will be held in the 2nd, 4th and 8th week of the 12-week study. Behavior Goals: Calorie: The calorie goal will be calculated from the individual's baseline body weight (1200 - 1800 kcal for <250 lbs or 1800 to 2000 kcal for >250 lbs). Calorie goals can be adjusted if necessary for participants struggling to meet the goa;s or for maintenance. Fat: Fat gram goals will 40 - 60 grams per day depending on calorie goal. Screening Measures - administered only at baseline. Sociodemographic Form will be used to collect data on individual characteristics, e.g., ethnicity, marital status. Rapid Eating Assessment for Patients (REAP) will be used to assess current diet to inform the goals for lifestyle improvement. It has 31 items that ask about weight, PA and sedentary habits, variety in diet, excess food intake. Participants Online Screening Questionnaire will be used to assess Qualtric systems as a screening tool. It will be given with the other screening questionnaires at their Baseline Assessment. Outcome or Dependent Measures. Unless otherwise noted, all measures will be conducted at 0 and 12 weeks. Trained staff will perform these in the Clinical Research Suite in the School of Nursing. Participants will be compensated for completing the 12-week assessment. BMI- Weight - measured with the Tanita Scale and Body Fat Analyzer with subjects in light clothing standing bare foot on the scale's footpads. Height (centimeters) measured with stadiometer for BMI (kg/m2) calculation. Cardiometabolic risk factors Blood pressure (BP). BP assessment will follow the standard AHA guidelines and measured using an Omron BP Monitor with ComFit cuff with the subject in a sitting position after at least a 5-min rest. Whole body composition. To describe % fat mass, we will measure body composition (fat mass, % fat, fat-free mass) by bioelectrical impedance analysis on the Tanita Scale and Body Fat Analyzer.120 Waist circumference will be measured twice with a Gullick II measuring tape. If the two values are within 2 cm of each other, a mean is calculated; if not, measurements are taken again until they are within 2 cm. Psychosocial surveys.
Weight Efficacy Lifestyle (WEL) is a 20-item scale used to assess level of confidence to resist eating in varied situations or emotional states. It has established psychometric properties 135 and takes 5 min to complete. This scale has added explanatory value in weight loss behavior in our previous studies. The Newest Vital Sign, a brief test of literacy applied to reading a food label. At the completion of study, the groups that were not randomized into the group sessions will receive the session material via email.
The group that did not receive feedback messages will be given the option of receiving messages for 12 weeks. If the participant chooses to have the feedback messages, it will be loaded on the participant's phones at the 12 weeks assessment.
- Conditions
- Overweight, Obesity
- Being tested
- Group Sessions, Feedback, Self-monitoring
- Keywords
- mobile technology, feedback message, self-monitoring
- Medical subject headings
- Overweight, Obesity
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Group SessionsBehavioural
Participants will receive a 3-session behavioral lifestyle program for a healthful lifestyle and weight loss.
FeedbackBehavioural
Participants will receive up to 4 daily feedback messages based on progress in attaining target behavior. The feedback messages will be delivered on a variable ratio schedule and tailored to data in subjects' dietary recordings.
Self-monitoringBehavioural
Participants will receive an one-time how to self-monitor using the smartphone session.
| Study group | Role | What they receive |
|---|---|---|
| Experimental: Group Sessions | Experimental | Participants will be asked to attend 3 group meetings over a 12 week period. Groups will meet for approximately 1 hour on weeks 2, 4 and 8. At each of the group meetings, the participant will be weighed and a group leader will present information on topics related to eating and exercise. Receives: Behavioral: Group Sessions; Behavioral: Feedback; Behavioral: Self-monitoring |
| Active Comparator: Self-Monitoring | Experimental | Active Comparator: Self-monitoring Participants will record diet, activity and weight as described above in the participant's smartphone app to assist the participant in losing weight. Receives: Behavioral: Self-monitoring |
| Experimental: Feedback | Experimental | Participants will be sent via the participant's smartphone between
1 and 4 feedback messages a day about whether the participant has been self monitoring, or the amount of calories, fat or sugar the participant has consumed. Receives: Behavioral: Feedback; Behavioral: Self-monitoring |
What is being measured
The primary outcome is the main question the study is designed to answer.
Change in weight
Changes in weight: measured as Percent change in weight from baseline to 12 weeks
Measured: 12 weeks
Secondary outcomes (2)
Adherence to treatment protocol
Number of days participants self-monitor
Measured: 12 weeks
Adherence to self-weighing protocol
Number of days participants self-weigh
Measured: 12 weeks
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted12 Jul 2016 (estimated)
- Study startMar 2015
- Primary completionMay 2015
- Study completionJun 2015
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for OverweightStudies of the same condition, open and under way.
- More trials run by University of PittsburghThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Factorial
- Masking
- None (open label)
- Enrolment
- 39 participants (actual)
Sponsor and investigators
- Lead sponsor
- University of Pittsburgh
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Lora Burke, University of Pittsburgh
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT02829632
- Sponsor's protocol ID
- PRO14110537
- Acronym
- SMARTER
- Status last verified
- Dec 2016
- First submitted
- 2 Jul 2015
- Last updated
- 5 Dec 2016
- Results posted
- No
- Data monitoring committee
- No
- Individual data sharing
- No: there is no plan to share the data. The data are being used for a grant application.
Publications
Metzendorf MI, Wieland LS, Richter B. Mobile health (m-health) smartphone interventions for adolescents and adults with overweight or obesity. Cochrane Database Syst Rev. 2024 Feb 20;2(2):CD013591. doi: 10.1002/14651858.CD013591.pub2.
PubMed 38375882
Study at a glance
From the registry record, last updated by the sponsor on 5 Dec 2016. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- 12 Weeks Weight Loss Study Using Feedback Messages Delivered Via Smartphone
- ClinicalTrials.gov ID
- NCT02829632
- Acronym / sponsor ID
- SMARTER / PRO14110537
- Conditions
- Overweight, Obesity
- Keywords
- mobile technology, feedback message, self-monitoring
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 39 participants (actual)
- Lead sponsor
- University of PittsburghUniversity, hospital or other
- Study start
- Mar 2015
- Primary completion
- May 2015 (actual)
- Study completion
- Jun 2015 (actual)
- First posted
- 12 Jul 2016 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
Brief Summary: This randomized clinical pilot will test the feasibility of having individuals self-monitor for 12 weeks and based on what the participants record be given feedback messages. The investigator will use this information to refine the questions and data collection procedures for the larger study.
Participants will be randomized into 3 groups
- self-monitoring only
- self-monitoring w/ feedback messages
- self-monitoring w/feedback messages and group sessions Feedback messages will be delivered up to 4 times per day using a different schedule. The group sessions will be held in the 2nd, 4th and 8th week of the 12-week study.
All participants will be asked to complete questionnaires and 2 assessment visits at baseline and 12 weeks.
Detailed description
Research Strategy. The investigator will randomize 45 overweight/obese adults to one of 3 groups: (1) Control (Con) - no FB, no Behavioral Lifestyle Program (BLP), (2) FB Only, no BLP, and (3) FB+BLP. All subjects will use a smartphone to self-monitor diet and PA. The subjects will download a feedback system onto the Android operating system smartphone that was developed for this study called the SMARTER. The algorithm was developed by Dr. Lora Burke of the University of Pittsburgh. All groups will attend a one-time how to self-monitor using the smartphone session and receive education materials at baseline. The FB Only and FB+BLP groups will receive up to 4 daily FB messages, based on progress in attaining target behavior. The FB will be delivered on a variable ratio schedule and tailored to data in subjects' recordings. FB+BLP participants will receive a face-to-face BLP intervention that will include 3 group sessions over 12 weeks. Also to not confound the effect of the daily FB, the interventionists will not provide feedback to the weekly diaries. Sample. The investigator will recruit from the community 45 adults, over the age of 18. All participants need to be randomized prior to the beginning of the 3 BLP sessions since the sessions are conducted as a closed group. The randomization scheme will be implemented via a computerized program (Visual Basic 6.0) using minimization method. The randomization will be overseen by a statistician (Co-I: S Sereika). Each of the 3 conditions will be assigned a total of 15 subjects with randomization stratified by gender and ethnicity/race. Intervention. Those in the Con and FB Only groups will receive a 1-hr session on provided calorie prescription for weight loss and self-monitoring and associated education materials. Only those in FB+BLP will receive a 3-session BLP for a healthful lifestyle and weight loss. The groups will meet in the School of Nursing and will be led by a trained interventionist. Protocol for Self-monitoring: All participants will be subscribed to LoseIt!, an online self-monitoring service that can be accessed via the smartphone and computer. This will be used in place of the traditional paper diary. This software permits self-monitoring of diet, PA, and weight; it also provides feedback on up to 9 macronutrients based on a database of 60,000 foods. Because of the investigator's ongoing working relationship with the developers of LoseIt! program, the investigator will have access to LoseIt! Connect, a custom portal created by LoseIt! for centralized user management. This permits the investigators to view participants' entries and set custom controls on participants use, (e.g., disabling particpants' ability to share data with outsiders). All participants will be encouraged to self-monitor diet and self-report weight. Participants who do not have scales will be given one for the duration of the study and be ask to return it at the completion of the study. Participants see the nutrient value of each food and the calculated subtotals. The interventionists will have access to the diaries so participants can contact a participant if there is any concern about the reported eating behaviors. This is the same procedure used for the past 4 years in the EMPOWER Study (IRB - PRO10100504). At the training session, participants will be advised on how to change the privacy settings on Lose It!. General Information about Feedback Algorithm. The FB algorithm programmed in the FB app will use real-time synced self- monitoring data to send messages that are responsive to the participants' entries. The server will deliver a message that will be displayed on the screen of the smartphones so the person does not need to make extra clicks to view it. The FB messages will address one target behavior at a time, e.g., self-monitoring or calorie intake. At the baseline education session for the FB Only group or the first BLP session for FB+BLP, the individual will make a diary entry; the system will send a FB message shortly thereafter to provide immediate reinforcement for self-monitoring. Then the FB will be delivered on the incremental 1-4 x/d schedule, contingent on progress in self-monitoring and in attaining the person's daily calorie goal. Rules will be applied to the delivery of messages to FB Only and FB+BLP, e.g., messages will be delivered between the hours set by the participants on particpants phone, e.g., 8 AM and 9:30 PM, and content will be guided by the parameters built into the algorithm. In the implementation of the proposed FB intervention, the investigators will exercise caution and sensitivity regarding participants' reception of the messages. In the SMART Trial, the messages were motivating and reinforcing, not noting deficiencies in behavior or progress not made; however, the messages will provide guidance for corrective action when the person is not following the behavior that would be consistent with the pre-established goals. Space does not permit extensive message samples but examples might be as follows. Excellent job on increasing fruits in your diet. OR Super job staying within the fat limits. Go easy on high fat foods tonight; consider having a big salad with nonfat dressing. Protocol for the Behavioral Lifestyle Program (BLP) intervention: Group Sessions: Participants will receive nutritional and behavioral counseling; practical hands-on experiences to develop skills to implement a healthy lifestyle (e.g., practice mindful eating, portion size, modify foods or meals to reduce fat content) in three 1 hour group sessions. The groups will meet evenings and will be led by the multidisciplinary team (behavioral scientists, nutritionists that has been trained by the PI and Co-I (Burke and Ewing). The group sessions will be held in the 2nd, 4th and 8th week of the 12-week study. Behavior Goals: Calorie: The calorie goal will be calculated from the individual's baseline body weight (1200 - 1800 kcal for <250 lbs or 1800 to 2000 kcal for >250 lbs). Calorie goals can be adjusted if necessary for participants struggling to meet the goa;s or for maintenance. Fat: Fat gram goals will 40 - 60 grams per day depending on calorie goal. Screening Measures - administered only at baseline. Sociodemographic Form will be used to collect data on individual characteristics, e.g., ethnicity, marital status. Rapid Eating Assessment for Patients (REAP) will be used to assess current diet to inform the goals for lifestyle improvement. It has 31 items that ask about weight, PA and sedentary habits, variety in diet, excess food intake. Participants Online Screening Questionnaire will be used to assess Qualtric systems as a screening tool. It will be given with the other screening questionnaires at their Baseline Assessment. Outcome or Dependent Measures. Unless otherwise noted, all measures will be conducted at 0 and 12 weeks. Trained staff will perform these in the Clinical Research Suite in the School of Nursing. Participants will be compensated for completing the 12-week assessment. BMI- Weight - measured with the Tanita Scale and Body Fat Analyzer with subjects in light clothing standing bare foot on the scale's footpads. Height (centimeters) measured with stadiometer for BMI (kg/m2) calculation. Cardiometabolic risk factors Blood pressure (BP). BP assessment will follow the standard AHA guidelines and measured using an Omron BP Monitor with ComFit cuff with the subject in a sitting position after at least a 5-min rest. Whole body composition. To describe % fat mass, we will measure body composition (fat mass, % fat, fat-free mass) by bioelectrical impedance analysis on the Tanita Scale and Body Fat Analyzer.120 Waist circumference will be measured twice with a Gullick II measuring tape. If the two values are within 2 cm of each other, a mean is calculated; if not, measurements are taken again until they are within 2 cm. Psychosocial surveys.
Weight Efficacy Lifestyle (WEL) is a 20-item scale used to assess level of confidence to resist eating in varied situations or emotional states. It has established psychometric properties 135 and takes 5 min to complete. This scale has added explanatory value in weight loss behavior in our previous studies. The Newest Vital Sign, a brief test of literacy applied to reading a food label. At the completion of study, the groups that were not randomized into the group sessions will receive the session material via email.
The group that did not receive feedback messages will be given the option of receiving messages for 12 weeks. If the participant chooses to have the feedback messages, it will be loaded on the participant's phones at the 12 weeks assessment.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Factorial
- Masking
- None (open label)
- Number of arms
- 3
| Arm | Type | Receives |
|---|---|---|
| Experimental: Group Sessions | Experimental | Behavioral: Group Sessions, Behavioral: Feedback, Behavioral: Self-monitoringParticipants will be asked to attend 3 group meetings over a 12 week period. Groups will meet for approximately 1 hour on weeks 2, 4 and 8. At each of the group meetings, the participant will be weighed and a group leader will present information on topics related to eating and exercise. |
| Active Comparator: Self-Monitoring | Experimental | Behavioral: Self-monitoringActive Comparator: Self-monitoring Participants will record diet, activity and weight as described above in the participant's smartphone app to assist the participant in losing weight. |
| Experimental: Feedback | Experimental | Behavioral: Feedback, Behavioral: Self-monitoringParticipants will be sent via the participant's smartphone between 1 and 4 feedback messages a day about whether the participant has been self monitoring, or the amount of calories, fat or sugar the participant has consumed. |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (5 listed)
- age 18 years or older
- BMI between 27-43
- have an Android smartphone,
- has not used app for self-monitoring at least 4 days/week for the past 3 months
- can attend group meetings.
Key exclusion criteria (7 listed)
- persons who plan to become pregnant
- have diabetes or a medical condition in which weight loss in contraindicated
- unable to walk for exercise
- on a weight loss drug
- had bariatric surgery
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| Group SessionsParticipants will receive a 3-session behavioral lifestyle program for a healthful lifestyle and weight loss. | Behavioural | Experimental: Group Sessions |
| FeedbackParticipants will receive up to 4 daily feedback messages based on progress in attaining target behavior. The feedback messages will be delivered on a variable ratio schedule and tailored to data in subjects' dietary recordings. | Behavioural | Experimental: Feedback, Experimental: Group Sessions |
| Self-monitoringParticipants will receive an one-time how to self-monitor using the smartphone session. | Behavioural | Active Comparator: Self-Monitoring, Experimental: Feedback, Experimental: Group Sessions |
Primary outcome
Change in weight
Time frame: 12 weeks
Changes in weight: measured as Percent change in weight from baseline to 12 weeks
2 secondary outcomes
Adherence to treatment protocol
Time frame: 12 weeks
Adherence to self-weighing protocol
Time frame: 12 weeks
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 5 Dec 2016.
- Derived from this study: PubMed 38375882Metzendorf MI, Wieland LS, Richter B. Mobile health (m-health) smartphone interventions for adolescents and adults with overweight or obesity. Cochrane Database Syst Rev. 2024 Feb 20;2(2):CD013591. doi: 10.1002/14651858.CD013591.pub2.
- Individual participant dataSharing planned: No. there is no plan to share the data. The data are being used for a grant application.
Related trials for Overweight
Recruiting
Preserving Muscle Mass During Incretin-Induced Weight Loss
Obesity (BMI > 35)
Not yet recruitingObservational study
A Natural History of Genetic and Environmental Predictors of Pubertal Timing Among Youth With Obesity
Obesity
Not yet recruitingObservational study
Assessing the Impact of Perceptions of Unpredictability on Objective Measures of Food Consumption and Metabolism
Healthy Volunteer, Obestity
Not yet recruitingPhase 2
Trial of the Combination of Alpha-Lipoic Acid and Mirabegron in Women and in Men With Obesity
Insulin Resistance, Obesity
Recruiting
Synchronous vs Asynchronous Remotely Delivered Lifestyle Interventions
Obesity
Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing Group Sessions, Feedback and Self-monitoring in people with Overweight and Obesity, run by University of Pittsburgh at 1 site in United States.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 5 inclusion and 7 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 5 Dec 2016. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Change in weight (time frame: 12 weeks). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT02829632, which also lists 1 linked publication.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 5 Dec 2016.