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ObesityNCT02616237

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

A study testing Lifestyle Intervention in people with Obesity, run by The Hong Kong Polytechnic University at 1 site in Hong Kong.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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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. Read more about this study

Who is it for?
Ages 18 to 60 years
Conditions the study is for
Obesity
What is being tested?
Lifestyle Intervention
Could I receive a placebo?
No, everyone receives an active treatment
How many people
59 participants
Where
1 siteHong Kong
Study dates
Apr 2014to Oct 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 to 60 years
  • All sexes
  • No healthy volunteers
  • Adult

Who may be able to join

  • 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.

Who cannot join

  • 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;
Show all 12Show fewer
  • 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 locations and contacts

1 site in 1 country.

Hong Kong1 site
  • The Hong Kong Polytechnic University

    Hong Kong

Other trials in Hong Kong

About this study

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

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.

Read the detailed 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

Conditions
Obesity
Being tested
Lifestyle Intervention
Keywords
Chinese population, acupressure, physical activity, nutrition, Facebook
Medical subject headings
Obesity, Motor Activity

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Lifestyle InterventionBehavioural

    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.

Study groups in NCT02616237
Study groupRoleWhat they receive
Intervention GroupExperimentalLifestyle 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.
Receives: Behavioral: Lifestyle Intervention
Control GroupNo interventionThe participants randomized into the Control Group will only receive government printed health information on healthy eating, physical activity, obesity and cancers.

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Changes in body weight

    Weights will be taken in light clothes without shoes using a digital scale

    Measured: Measures are done in three time points: baseline, 3 months and 6 months

  2. 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)

    Measured: Measures are done in three time points: baseline, 3 months and 6 months

  3. Changes in waist circumference

    Waist circumference will be measured by using an inelastic tape measure

    Measured: Measures are done in three time points: baseline, 3 months and 6 months

Secondary outcomes (7)
  1. 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)

    Measured: Measures are done in three time points: baseline, 3 months and 6 months

  2. Changes in weight self-efficacy

    Self-efficacy for weight loss will be assessed by using a 20-item Weight Efficacy Lifestyle Questionnaire (WEL).

    Measured: Measures are done in three time points: baseline, 3 months and 6 months

  3. 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.

    Measured: Measures are done in three time points: baseline, 3 months and 6 months

  4. 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

    Measured: Measures are done in three time points: baseline, 3 months and 6 months

  5. 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

    Measured: Measures are done in three time points: baseline, 3 months and 6 months

  6. 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

    Measured: Measures are done in three time points: baseline, 3 months and 6 months

  7. Changes in physical activity

    The International Physical Activity Questionnaire will be used to assess the changes in physical activity

    Measured: Measures are done in three time points: baseline, 3 months and 6 months

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted26 Nov 2015 (estimated)
  2. Study startApr 2014
  3. Primary completionOct 2015

Resources

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
Parallel groups
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
59 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02616237
Sponsor's protocol ID
20131213002
Status last verified
Aug 2016
First submitted
24 Nov 2015
Last updated
24 Aug 2016
Results posted
No
Data monitoring committee
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Lifestyle Intervention in people with Obesity, run by The Hong Kong Polytechnic University at 1 site in Hong Kong.

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 6 inclusion and 12 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 24 Aug 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 Hong Kong. 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?

Changes in body weight (time frame: Measures are done in three time points: baseline, 3 months and 6 months). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
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 24 Aug 2016.

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