Use of Wearable Tech to Increase Physical Activity in Inpatient Rehabilitation for Overweight and Obese Patients
NCT ID: NCT04031079
Last Updated: 2020-01-27
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
NA
37 participants
INTERVENTIONAL
2019-08-12
2020-01-13
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Comparison of a Technology-based System and an In-person Behavioral Weight Loss Intervention in the Severely Obese
NCT01537796
The Effect of HealthWear on Short-Term Weight Loss
NCT00177593
Rehabilitating Overweight People Back to Working Life
NCT01361490
Lifestyle Intervention in Morbidly Obese Patients
NCT00464984
Effect Evaluation of the Work Rehabilitation Effort "Best iLag"
NCT02945397
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
The feedback application will give participants in the intervention group information about the number of PAI they earn each week. PAI is short for Personal Activity Intelligence. One earns PAI points every time heart rate increases: The higher heart rate, the faster one earns PAI. Previous research have shown that those who achieve 100 PAI or more every week over time, live for an average of more than eight years longer than others.
During the study all participants will take part in a traditional inpatient rehabilitation program (lifestyle modification program). The program consist of three periods at the rehabilitation center with time at home in-between. The study will take place during two periods at the center and one period at home. Time spent on physical activity and number of earned PAI's will be counted during the period at home.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Wearable tech with feedback
This group will be wearing an activity measurement device (wristband) and receive feedback about their activity level through a mobile application while taking part in a traditional inpatient rehabilitation program for overweight and obesity (lifestyle change program).
Wearable tech with feedback
an armwrist device measuring physical activity level. The user will receive information about their physical activity level through their smartphone
Rehabilitation program
traditional inpatient rehabilitation program for overweight and obesity (lifestyle change program)
Wearable tech without feedback
This group will be wearing the same the activity measurement device as the intervention group, but they will not receive any feedback about their activity level. They will not have access to the mobile application. They will take part in the same rehabilitation program as the intervention group.
Wearable tech without feedback
an armwrist device measuring physical activity level, no reporting back to the user
Rehabilitation program
traditional inpatient rehabilitation program for overweight and obesity (lifestyle change program)
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Wearable tech with feedback
an armwrist device measuring physical activity level. The user will receive information about their physical activity level through their smartphone
Wearable tech without feedback
an armwrist device measuring physical activity level, no reporting back to the user
Rehabilitation program
traditional inpatient rehabilitation program for overweight and obesity (lifestyle change program)
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* having been referred from a hospital outpatient obesity clinic.
Exclusion Criteria
* using a wheelchair (the technology will be not able to measure activity correctly)
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Norwegian University of Science and Technology
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Lene Aasdahl, PhD MD
Role: PRINCIPAL_INVESTIGATOR
National Taiwan Normal University
Jorunn Helbostad, Dr Philos
Role: STUDY_DIRECTOR
Norwegian University of Science and Technology
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Unicare Helsefort
Rissa, , Norway
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
2019/799
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.