THERMACTIVE: Impact of Web and Smartphone-based Physical Activity Program on Physical Activity Level 12 Months After a Balneotherapy

Sponsor
Association Francaise pour la Recherche Thermale (Other)
Overall Status
Completed
CT.gov ID
NCT02694796
Collaborator
(none)
230
9
2
27.6
25.6
0.9

Study Details

Study Description

Brief Summary

The purpose of this study is to evaluate the impact of an intervention combining a workshop during a balneotherapy and the use after the end of the balneotherapy of a web and smartphone-based physical activity program using connected devices, on physical activity level among patients 12 months after they participated in a balneotherapy in thermal care center.

A multi center randomized controlled trial is setting to evaluate the impact of the intervention on physical activity recommendations achievement of the patients.

Investigators hypothesize that an intervention including a workshop during a balneotherapy and an automated physical activity program using web, mobile phone and connected devices will help patients to be engaged in more physical activities and to reach physical activity recommendations.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Physical activity program after a balneotherapy
N/A

Detailed Description

New technologies such as mobile phone and connected devices have been recognized as useful tools to assist chronic patients in their disease's management. they are also considering as promising tools to help patients to change their lifestyle behavior.

Balneotherapy is a very special moment to initiate changes and to raise awareness about healthier behavior in terms of food and physical activity.

The objective of the intervention is to help patients with chronic diseases, taking part in a balneotherapy, to increase or maintain their physical activity level in the long term to reach the national recommendations of 150 minutes of moderate physical activity per week.

Patients will be randomized either in the intervention group or in the control group.

The intervention group will participate in a workshop during the balneotherapy providing them informations about physical activity and also about the way to use the web and smartphone-based physical activity program along with the use of the connected devices (scale and pedometer). After the end of the balneotherapy, the intervention group will have access to the web and smartphone-based physical activity program during 12 months.

The control group will receive a booklet including informations about physical activity practice.

Study Design

Study Type:
Interventional
Actual Enrollment :
230 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Outcomes Assessor)
Primary Purpose:
Supportive Care
Official Title:
Long Term Impact of a Physical Activity Intervention Combining Workshop During a Balneotherapy and a Web and Smartphone-based Physical Activity Program After Balneotherapy, on Physical Activity Level : a Randomized Control Trial
Study Start Date :
Sep 1, 2015
Actual Primary Completion Date :
Dec 20, 2017
Actual Study Completion Date :
Dec 20, 2017

Arms and Interventions

Arm Intervention/Treatment
Experimental: Intervention

The 'Physical activity program after a balneotherapy' intervention involves providing a workshop during a balneotherapy about physical activity and use of automated physical activity program including website, mobile app and connected devices, and after the balneotherapy, the access to the automated program during 12 months.

Behavioral: Physical activity program after a balneotherapy
workshop during the balneotherapy associated to an automated program of physical activity after the end of the balneotherapy available during 12 months

No Intervention: Control

Patients included in the control arm will receive a booklet including informations about physical activity recommendations and practice.

Outcome Measures

Primary Outcome Measures

  1. Achievement of Physical activity recommendations [at 12 months of follow-up]

    Proportion of patients in each arm of the study (intervention and control) who achieve physical activity recommendations. Physical activity will be measured by IPAQ questionnaire (International Physical Activity Questionnaire). Achievement of physical activity recommendations corresponds to 150 minutes of moderate physical activity per week. To compare physical activity at 12 months, a constrained Longitudinal Data Analysis will be used involving the repeated measure of physical activity at inclusion and every 2 months until the end of the 12 months of follow-up.

Secondary Outcome Measures

  1. Physical activity [at inclusion, 6 and 12 months of follow-up]

    IPAQ questionnaire to evaluate in each arm of the study physical activity (like physical activity level, sedentary time, the proportion of patients reporting an increase of at least 20 minutes of moderate physical activity per week)

  2. Weight [at inclusion, 6 and 12 months of follow-up]

  3. Waist circumference [at inclusion, 6 and 12 months of follow-up]

  4. Quality of life [at inclusion, 6 and 12 months of follow-up]

    The quality of life will be measured thanks to the SF-12 questionnaire (Short Form Health Survey)

  5. Captured physical activity [at return home after the end of the balneotherapy, at 6 months and at 12 months of follow-up]

    Physical activity will be measured thanks to accelerometers integrated into smartphones

Eligibility Criteria

Criteria

Ages Eligible for Study:
50 Years to 79 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • age between 50 and 79

  • BMI between 19 and 35 kg.m2

  • stabilized chronic disease : cardiovascular disease, obesity, diabetes, chronic obstructive pulmonary disease, rheumatic diseases, breast cancer

  • practice of moderate physical activity less than 150 minutes per week

  • practice of sportive activity less than 2h per week

  • having access to internet

  • possessing a smartphone connected to internet

  • good comprehension of french

  • notice and informed consent signed

  • no contraindication to practice physical activity

  • subject to French Social Security

Exclusion Criteria:
  • wearing a cardiac pacemaker

  • non-stabilized chronic disease

  • invalidating pathology of locomotor system

  • metastatic cancers

  • being in an exclusion period for participating in another study or having received more than 4500€ during the year due to participation in clinical studies

  • being under supervision

  • refusing to be register in the French National Volunteers Register

Contacts and Locations

Locations

Site City State Country Postal Code
1 Thermes CHEVALLEY Aix-les-Bains France 73100
2 Centre thermal d'Amélie-les-Bains Amélie-les-Bains France 66110
3 Thermes de Bourbon-Lancy Bourbon Lancy France 71140
4 Thermes de Brides-les-Bains Brides-les-Bains France 73573
5 Caleden Complexe Thermal Chaudes-Aigues France 15110
6 Centre thermal d'Eugénie-les-Bains Eugénie-les-Bains France 40320
7 Thermes du Boulou Le Boulou France 66160
8 Thermes de Vals-les-Bains Vals-les-Bains France 07600
9 Thermes CALLOU Vichy France 03200

Sponsors and Collaborators

  • Association Francaise pour la Recherche Thermale

Investigators

  • Principal Investigator: Martine DUCLOS, MD-PhD, Centre Hospitalier Universitaire Gabriel Montpied, Clermont Ferrand

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Association Francaise pour la Recherche Thermale
ClinicalTrials.gov Identifier:
NCT02694796
Other Study ID Numbers:
  • C2015/02
First Posted:
Mar 1, 2016
Last Update Posted:
Jun 29, 2018
Last Verified:
Jun 1, 2018
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Keywords provided by Association Francaise pour la Recherche Thermale
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jun 29, 2018