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Exercise Consultation for Type 2 Diabetes Patients in Real Life

Does Exercise Consultation Have a Realistic Chance of Increasing the Physical Activity Level of Type 2 Diabetes Patients in Real Life?

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01264809
Acronym
APDT 2
Enrollment
80
Registered
2010-12-22
Start date
2011-03-31
Completion date
2013-03-31
Last updated
2010-12-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diabetes Mellitus, Type 2

Keywords

diabetes

Brief summary

The prevalence of type 2 diabetes is high and expected to increase dramatically in worldwide, in France and especially in the French West Indies.This chronic disease is associated with premature mortality and various debilitating complications which can be prevented by optimal control of glycaemia, blood pressure and lipids. Diabetes management includes lifestyle modification and medication. Despite numerous studies supporting the benefits of frequent physical activity for people with Type 2 diabetes, an estimated 60±80% of this population remain sedentary. Promotion of physical activity in current diabetes care seems to be inadequate. The aim of this randomized controlled trial is to evaluate the medium-term effectiveness (after 3 and 6months) of exercise consultation in promoting physical activity in outpatients with Type 2 diabetes.

Interventions

BEHAVIORALSpecific consultation for physical activity counseling

Specific consultation

BEHAVIORALConsultation for physical activity counseling

Specific consultation

Sponsors

Clinique Antilles-Guyane
CollaboratorOTHER
University Hospital Center of Martinique
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

* Type 2 DM diagnosed within 10 years prior the inclusion * 18-70 years old * Signed written informed consent * Diabetes treatment regimens : * diet only * oral antidiabetic drug * oral antidiabetic drugs with long acting insulin analog * oral antidiabetic drugs with GLP 1 analog

Exclusion criteria

* Minors * Patients with concurrent medical conditions preventing exercise * Pregnancy or intention to become pregnant during the study * Inability to read and write French * History of participating in our education program during the past two years * Usual sporty activities * Change in diabetes treatment during the three months prior to study enrollment * No written informed consent

Design outcomes

Primary

MeasureTime frame
Change in daily physical activity measured by SenseWear Pro3 Armband®. Participants were instructed to wear the monitor for seven days during all waking hours except bathing.3 months

Secondary

MeasureTime frameDescription
Benefits obtained after the physical activity counseling6 monthsThe secondary outcome of this study is to compare the benefits obtained 3 and 6 mounths after the physical activity counseling on : * Quality of life scores * Anthropometric measurement and Body Mass Index (BMI) * Body composition measurement * Hand grip strength * Blood pressure * Glycaemic control and cholesterol * Medication

Countries

France

Contacts

Primary ContactJocelyne CRASPAG
jocelyne.craspag@chu-fortdefrance.fr(0)596592698
Backup ContactMickaëlle ROSE
mickaelle.rose@chu-fortdefrance.fr(0) 596592698

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026