- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05276544
The Effect of Telephone and Video Counseling on Weight Loss and Quality of Life
The Effect of Telephone and Video Counseling Given to Obese Individuals on Weight Loss and Quality of Life in the COVID-19 Pandemic: an RCT
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
The use of phone/video consultancy applications for body weight control and diet monitoring is increasing. One of the main reasons for this situation is that individuals care more about the social distance rule as a result of the increase in health concerns after the COVID-19 (SARS-CoV-2) pandemic. In addition, due to the uncertainty of how long the pandemic will last, many people are adapting to online applications and programs quicly. However, it's unclear which method of phone/video-based diet counseling is more successful or preferable to traditional diet follow-up. Based on the above-mentioned information; in this study, it is aimed to determine the effect of diet counseling via phone or video on weight loss and to compare it with the traditional follow-up method in the COVID-19 pandemic.
Individuals who meet the research criteria will randomize according to their file numbers (with the ramdomizer program) and divide into 3 groups: telephone counseling (15), video counseling (15) and traditional follow-up group (Figure 1.). Food consumption records, anthropometric measurements and quality of life scale scores of all individuals will record at the beginning and end of the study (Figure 2.). In order to prevent interaction between individuals, all diet programs will prepare at different times and individually.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
-
Ankara, Turkey, 06000
- Ümüş Özbey
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Being between the ages of 20-65
- Being obese (BMI≥30 kg/m2)
- Having a smartphone with internet access and being competent to use it
- Volunteering to participate in research
Exclusion Criteria:
- Being pregnant/lactating
- Having a hearing problem
- Being on a followed diet program
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Sequential Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: phone counseling
dietary intervention via phone counseling
|
Dietary intervention: Preparation and follow-up of diet program.
|
|
Experimental: video counseling
dietary intervention via video counseling
|
Dietary intervention: Preparation and follow-up of diet program.
|
|
Experimental: Traditional follow up
dietary intervention via traditional follow up
|
Dietary intervention: Preparation and follow-up of diet program.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Weight chance
Time Frame: At the end of the 3 months
|
BMI (kilogram/ metre2 (kg/m2))
|
At the end of the 3 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Quality of Life Score
Time Frame: At the end of the 3 months
|
The score ranges from 0 to 100 points, with an increased score reflecting improved quality of life
|
At the end of the 3 months
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: ümüş Ö yücel, Dr, Ankara University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- AmasyaUniv
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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