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Clinical Trial Details — Status: Active, not recruiting

Administrative data

NCT number NCT04219800
Other study ID # 2019-05383
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date December 8, 2020
Est. completion date December 30, 2024

Study information

Verified date January 2024
Source Umeå University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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)


Recruitment information / eligibility

Status Active, not recruiting
Enrollment 142
Est. completion date December 30, 2024
Est. primary completion date December 30, 2023
Accepts healthy volunteers No
Gender All
Age group 40 Years to 64 Years
Eligibility Inclusion Criteria: - Type 2 Diabetes Melltitus - 40-64 years - HbA1c 48-100 mmol/mol - BMI = 25 kg/m2 - Working at least 75% of full-time in a mainly seated job. Exclusion Criteria: - Pregnancy - Regular vigorous intensity exercise - Severe disease or for other reason unable to follow the study protocol

Study Design


Related Conditions & MeSH terms


Intervention

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

Locations

Country Name City State
Sweden Hallsbergs hälsocentral Hallsberg
Sweden Kärna Vårdcentral Linköping
Sweden Björkskatans Hälsocentral Luleå Norrbotten
Sweden Clinical Research Centre Östersund
Sweden Torsviks Vårdcentral Stockholm
Sweden Clinical Research Centre Umeå

Sponsors (8)

Lead Sponsor Collaborator
Umeå University Norrbottens County Council, Region Jämtland Härjedalen, Region Örebro County, Region Östergötland, Region Stockholm, Region Västerbotten, Vastra Gotaland Region

Country where clinical trial is conducted

Sweden, 

Outcome

Type Measure Description Time frame Safety issue
Other General self-efficacy GSE-10 questionnaire 12 months
Primary Sitting time Assessed by activPAL3 thigh-worn accelerometer 12 months
Secondary Steps Assessed by activPAL3 thigh-worn accelerometer 12 months
Secondary Fatigue MFI-20 questionnaire 12 months
Secondary Health-related quality of life RAND-36 questionnaire 12 months
Secondary Cardiometabolic composite score (CCMR) Will be determined by summing z-scores ([value-mean]/SD) of waist circumference (cm), mean arterial pressure (mmHg), HbA1c (mmol/mol), the inverse of HDL (mmol/L) and triglycerides (mmol/L), using sex-specific means and SDs 12 months
Secondary Sick leave Assessed by diary 12 months
Secondary Medications Total use of medications 12 months
Secondary Musculoskeletal problems NRS questionnaire 12 months
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