Feasibility and Preliminary Efficacy of a Theory-driven BALANCE Dietary Program Among Patients With Type 2 Diabetes

NCT07472855 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30

Last updated 2026-03-16

No results posted yet for this study

Summary

This study explores the effect of an individualized dietary intervention program based on COM-B theory on improving health outcomes in patients with T2DM, improvement in metabolic health indicators and an increased diabetes remission rate, as well as changes in dietary adherence, self-management ability, and self-efficacy.

Conditions

Interventions

BEHAVIORAL

Psychological capability education

Intensified education on diabetes knowledge

BEHAVIORAL

Physical capability education

Intensified training in practical skills for dietary management

BEHAVIORAL

motivation management

action planning, behavior goal setting, problem solving, reward mechanisms, and establishing role models

BEHAVIORAL

support and supervision

empowerment management via a WeChat group, social support, and guidance based on indicator monitoring on the clinician side of a mini-program

BEHAVIORAL

A standardized diabetes care

a routine dietary management model will be implemented, including health guidance, WeChat group management, and supervision and management

Sponsors & Collaborators

  • The Luhe Teaching Hospital of the Capital Medical University

    collaborator OTHER
  • Capital Medical University

    lead OTHER

Principal Investigators

  • Ji Meihua · Capital Medical University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Model
PARALLEL

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-06-01
Primary Completion
2025-12-01
Completion
2025-12-01

Countries

  • China

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07472855 on ClinicalTrials.gov