A Facebook-based Weight Loss Programme for Obese Adults in Hong Kong

Obesity Clinical Trial

Official title:

Effects of a Facebook-based Weight Loss Programme for Obese Adults in Hong Kong

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02616237
• Other study ID #: 20131213002
• Status: Completed
• Phase: N/A
• First received: November 24, 2015
• Last updated: August 22, 2016
• Start date: April 2014

Study information

• Verified date: August 2016
• Source: The Hong Kong Polytechnic University
• Contact: n/a
• Is FDA regulated: No
• Health authority: Hong Kong: The Hong Kong Polytechnic University
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to determine the feasibility and efficacy of a 6-month weight loss intervention program for obese working adults through a popular social networking site - Facebook.

Description:

Obese individuals often are at higher risk for developing non-communicable diseases such as diabetes and cardiovascular disease. The regular physical activity, healthy diet and social support have been shown to be beneficial for weight loss.

This is a two-arm parallel design randomized controlled trial for 6 months. Participants who completed the baseline assessment will be randomly allocated, after stratified by gender, to either a control group or Facebook-based intervention group. The control group will receive information on healthy eating, physical activity, obesity and cancer via three government printed health pamphlets. In addition to the government health pamphlets, the intervention group will receive a programme delivered through Facebook.

The interventions include participation in a private research group on Facebook for health education, self monitoring and social support. Participants will receive 12 weekly lessons related to nutrition, physical activity, Chinese food therapy, acupressure, weight loss. A registered nutritionist and a registered Chinese medicine practitioner will join the Facebook group as health partners. Both of them are also registered nurses.

Data collection will be carried out at baseline, 3 months and 6 months. Each time, both groups will complete online questionnaires and attend in-person anthropometric measurements

Recruitment information / eligibility

• Status: Completed
• Enrollment: 59
• Est. primary completion date: October 2015
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 60 Years

Eligibility

Inclusion Criteria:

• university full-time employees;

• age 18 to 60 years,

• BMI of 25 to 40 kg/m2,

• have access to Internet and Facebook;

• able to communicate in both English and Chinese at F.5 secondary school level or above.

• agree to communicate with Internet, email, Facebook group and respect privacy.

Exclusion Criteria:

• Smoker;

• an unstable medical or mental status;

• history of myocardial infarction or stroke, or cancer in the past 5 years;

• orthopedic or joint problems that would prohibit exercise;

• in treatment for alcohol or drug dependency;

• an eating disorder;

• pregnant, breastfeeding, or planning on becoming pregnant within the next 6 months;

• use of medication that might affect body weight;

• a recent weight loss of more than 4.5 kg in the previous 6 months;

• currently participating in a weight loss program;

• organic obesity;

• unable to attend assessments or increase physical activity.

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind (Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

• Obesity
• Weight Loss

Intervention

Behavioral:
• Lifestyle Intervention
East-meets-West Lifestyle Intervention elements include nutrition and exercise from the Western perspective, food therapy and acupressure from the Traditional Chinese Medicine perspective, self-monitoring, and motivational videos of successful stories from working colleagues. The group participants in the Facebook are encouraged to post their health behaviors and questions, self-monitor, pledge for weight loss, seek social support and interact with health partners and other participants.

Locations

Country	Name	City	State
Hong Kong	The Hong Kong Polytechnic University	Hong Kong

Sponsors (1)

Lead Sponsor	Collaborator
The Hong Kong Polytechnic University

Country where clinical trial is conducted

Hong Kong, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Changes in body weight	Weights will be taken in light clothes without shoes using a digital scale	Measures are done in three time points: baseline, 3 months and 6 months	No
Primary	Changes in Body Mass Index	Height will be taken at baseline using a wall-mounted stadiometer. BMI will be calculated as weight (kg)/height (m2)	Measures are done in three time points: baseline, 3 months and 6 months	No
Primary	Changes in waist circumference	Waist circumference will be measured by using an inelastic tape measure	Measures are done in three time points: baseline, 3 months and 6 months	No
Secondary	Changes in Stages of Change	A 5-item questionnaire will be used to categorize participants into stages of change (pre-contemplation, contemplation, preparation, action, maintenance)	Measures are done in three time points: baseline, 3 months and 6 months	No
Secondary	Changes in weight self-efficacy	Self-efficacy for weight loss will be assessed by using a 20-item Weight Efficacy Lifestyle Questionnaire (WEL).	Measures are done in three time points: baseline, 3 months and 6 months	No
Secondary	Changes in physical activity self-efficacy	A questionnaire of perceived confidence to engage in physical activity under a variety of circumstances on a 5-point Likert scale will be used.	Measures are done in three time points: baseline, 3 months and 6 months	No
Secondary	Changes in weight decisional balance	A 20-item questionnaire of perceived pros and cons of weight loss on a 5-point Likert scale. The balance of the two scores >0 indicate more advantages than disadvantages to weight loss	Measures are done in three time points: baseline, 3 months and 6 months	No
Secondary	Changes in social support	A questionnaire will be used to measure the perceived support and sabotage from friends and family for healthy eating and physical activity	Measures are done in three time points: baseline, 3 months and 6 months	No
Secondary	Changes in dietary intake of fruits and vegetables	A questionnaire will be used to assess self-reported intake of fruits and vegetables in terms of portion size and frequency	Measures are done in three time points: baseline, 3 months and 6 months	No
Secondary	Changes in physical activity	The International Physical Activity Questionnaire will be used to assess the changes in physical activity	Measures are done in three time points: baseline, 3 months and 6 months	No