Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID06209996

Lose Little, Live Longer: A Randomised Controlled Feasibility Trial of a Diet and Exercise Weight Management Intervention for Overweight Chinese Cancer Survivors

Led by The University of Hong Kong · Updated on 2025-06-11

102

Participants Needed

1

Research Sites

25 weeks

Total Duration

On this page

Sponsors

T

The University of Hong Kong

Lead Sponsor

H

Health and Medical Research Fund

Collaborating Sponsor

AI-Summary

What this Trial Is About

This research aims to assess the feasibility and acceptability of a randomized controlled trial evaluating an adaptive weight management intervention for Chinese cancer survivors who are overweight or obese after completing their cancer survivorship care. The study focuses on improving body weight, BMI, dietary quality, physical activity, physical and psychosocial functioning, self-efficacy for weight loss, and quality of life. It follows guidelines for feasibility trials without setting hypotheses, as the main goal is to prepare for a larger trial. The trial has three study groups: the experimental group receives the Lose Little, Live Longer (L4) weight management intervention, a therapist-led program delivered in group phone sessions over five weeks focusing on diet, exercise, self-efficacy, and craving management. The active control group receives five weekly educational videos promoting balanced diet and physical activity through instant messaging. The waitlist control group receives pamphlets with general diet and activity information and will be offered the L4 intervention after the study. Participants will be assessed at baseline, immediately post-intervention, and at 3 and 6 months post-intervention for outcomes including recruitment and retention rates, adherence, weight and BMI changes, self-efficacy, dietary assessment, skin carotenoid status, physical activity, and quality of life measures. The study includes questionnaires, physical and psychosocial evaluations, and tracking of missing data. The total participation duration covers intervention delivery and follow-up assessments extending to six months post-intervention.

CONDITIONS

Brief Title

A Weight Management Intervention for Overweight Chinese Cancer Survivors

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Chinese cancer survivors attending a one-time face-to-face survivorship care clinic
  • Cantonese- or Mandarin-speaking individuals
  • Aged 18 years or older
  • Diagnosed with early-stage cancer (stage 0 to II)
  • Completed primary and adjuvant treatments such as chemotherapy and radiotherapy
  • Body mass index (BMI) of 23 kg/m2 or higher at 3-month reassessment, indicating overweight or obesity according to Asia-Pacific BMI cutoffs
Not Eligible

You will not qualify if you...

  • Non-Chinese cancer survivors with advanced or metastatic disease
  • Individuals with communication difficulties
  • Individuals with mobility impairments
  • Individuals with cognitive disabilities

AI-Screening

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 5 weeks

Participants receive a weight management intervention involving weekly group sessions or educational videos designed to improve diet and physical activity over five weeks.

5 weekly visits (remote or group sessions depending on assigned intervention)

Follow-up

Duration - 6 months

Participants are followed for up to 6 months after the intervention to monitor changes in weight, BMI, dietary habits, physical activity, and quality of life.

3 visits at immediate post-intervention, 3 months, and 6 months post-intervention

Trial Site Locations

Total: 1 location

1

The University of Hong Kong Jockey Club Institute of Cancer Care

Hong Kong, Hong Kong

Actively Recruiting

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Research Team

D

Danielle Ng, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

QUADRUPLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

3

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