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

T

The Hong Kong Polytechnic University

Status

Completed

Conditions

Obesity

Treatments

Behavioral: Lifestyle Intervention

Study type

Interventional

Funder types

Other

Identifiers

NCT02616237
20131213002

Details and patient eligibility

About

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.

Full 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

Enrollment

59 patients

Sex

All

Ages

18 to 60 years old

Volunteers

No Healthy Volunteers

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.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

59 participants in 2 patient groups

Intervention Group
Experimental group
Description:
Lifestyle Intervention: 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. Besides the Facebook contents, the participants will also receive government printed health information on healthy eating, physical activity, obesity and cancers.
Treatment:
Behavioral: Lifestyle Intervention
Control Group
No Intervention group
Description:
The participants randomized into the Control Group will only receive government printed health information on healthy eating, physical activity, obesity and cancers.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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