Reduced Occupational Sitting in Type 2 Diabetes Using mHealth (Mobile Health)

NCT04219800 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 46

Last updated 2026-05-19

No results posted yet for this study

Summary

Type 2 diabetes mellitus (T2DM) patients are suboptimal treated due to low uptake of physical activity. Recent research shows promising beneficial health effects from reducing sitting time by regular short bouts of light-intensity physical activity. These findings open up for a new focus in T2DM treatment but conclusive evidence is missing as studies have been short-term trials, mainly conducted in laboratory environments. Recent research suggest that reduced sitting and increased physical activity can be supported at a low cost by mHealth (mobile health) technology such as activity tracker armbands that warns of prolonged sitting and SMS text messages that reminds of activity breaks.

The overarching purpose of the project is to evaluate the effects of an intervention aimed to reduce occupational sitting in T2DM using mHealth (mobile health). It is hypothesized that the intervention will lead to (1) Activity changes - reduced sitting time and/or increased number of steps (primary outcome measures) and (2) Health effects - lower fatigue, improved health-related quality of life, reduced cardiometabolic risk, less sick leave, less medication, less musculoskeletal problems (secondary outcome measures)

Conditions

  • Diabetes Mellitus, Type 2

Interventions

BEHAVIORAL

Patient-centered counselling and written material

Patient-centered counselling and written material regarding occupational sedentary behaviour, with telephone follow-ups after 1 and 5 weeks.

BEHAVIORAL

mHealth

1. Activity tracker armband (Garmin Vivofit); warns of prolonged sitting and counts daily steps. 2. SMS text messages; reminds of activity breaks. 3. Mobile video instruction for standing pause gymnastics.

Sponsors & Collaborators

  • Norrbottens County Council

    collaborator OTHER_GOV
  • Vastra Gotaland Region

    collaborator OTHER_GOV
  • Region Östergötland

    collaborator OTHER
  • Region Stockholm

    collaborator OTHER_GOV
  • Region Örebro County

    collaborator OTHER
  • Region Västerbotten

    collaborator OTHER_GOV
  • Region Jämtland Härjedalen

    collaborator OTHER
  • Umeå University

    lead OTHER

Principal Investigators

  • Patrik Wennberg · Umeå University

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
40 Years
Max Age
64 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2020-12-08
Primary Completion
2023-12-30
Completion
2024-12-30

Countries

  • Sweden

Study Locations

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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 NCT04219800 on ClinicalTrials.gov