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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT02803489
Other study ID # ALMED-14-MD-051
Secondary ID
Status Terminated
Phase N/A
First received May 23, 2016
Last updated May 11, 2017
Start date April 8, 2016
Est. completion date May 9, 2017

Study information

Verified date April 2017
Source Air Liquide Santé International
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Prospective, non-randomized, open-label, pilot study conducted in a single group of 30 evaluable patients, i.e. patients completing an approximate 3 month follow-up.


Description:

The eHealth system developed in the present study is dedicated to multimorbid patients' follow-up. The medical device consists in Telemonitoring, Telenotification and Telecoaching. It aims to both increase patient autonomy, with regard to management of his/her pathologies, and facilitate coordination between health professionals.

By providing patients with tools enabling early detection of clinical worsening combined with an appropriate management, the medium and long-term objectives are to reduce hospitalizations and improve health status and quality of life of these patients at home.

In the first instance, the only objective of the present study is to evaluate the performance and feasibility of implementation of the device. This evaluation is based on a comparison between the telenotifications generated by the software and those calculated from the raw data captured by the software.


Recruitment information / eligibility

Status Terminated
Enrollment 23
Est. completion date May 9, 2017
Est. primary completion date March 23, 2017
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

Patients presenting all the following characteristics are eligible for inclusion:

1. Adult (>18 yrs), male or female

2. Presenting at least two chronic diseases among the following three: chronic heart failure (CHF), chronic obstructive pulmonary disease (COPD), diabetes

3. Having been hospitalized in the CHANGE or in any other medical care center (hospital or private clinic) for acute decompensation of CHF or exacerbation of COPD at least once during the 12 months prior to inclusion

4. Able to speak and understand French to a satisfactory standard

5. Having a phone land line

6. Capable of understanding and accepting the study constraints

7. Having signed a written informed consent after a full explanation of the study by the investigator prior to inclusion

Exclusion Criteria:

Patients presenting any one of the following characteristics are not eligible for inclusion:

1. Pregnant or breast-feeding woman

2. Institutionalized

3. Having a life expectancy of less than 3 months

4. Receiving or having received chemotherapy or radiotherapy for cancer within the past 6 months

5. Undergoing dialysis for chronic renal insufficiency

6. Presenting a condition likely to hamper accomplishment of the study procedures, such as chronic alcoholism, drug or solvent addiction, uncontrolled psychiatric disease or severe cognitive deficiency

7. Not covered by French Social Security

8. Participating or having participated in another interventional trial within the past 30 days

Study Design


Related Conditions & MeSH terms


Intervention

Device:
medical device intervention


Locations

Country Name City State
France Cabinet Privé de Cardiologie - 2, rue jean jaurès Annecy
France Cabinet Privé de Pneumologie - 7 rue gabriel de mortillet Annecy
France Centre Hospitalier d'Annecy Genevois - service cardiologie - 1 avenue de l'Hôpital BP 90074 Metz-Tessy PRINGY Cedex
France Centre Hospitalier d'Annecy Genevois - service pneumologie - 1 avenue de l'Hôpital BP 90074 Metz-Tessy Pringy cedex
France Cabinet privé de pneumologie - 28 avenue de Genève Saint Julien en Genevois
France cabinet privé de médecine générale - 18, rue Louis Haase Thones

Sponsors (2)

Lead Sponsor Collaborator
Air Liquide Santé International INFERENTIAL

Country where clinical trial is conducted

France, 

References & Publications (27)

Barnett K, Mercer SW, Norbury M, Watt G, Wyke S, Guthrie B. Epidemiology of multimorbidity and implications for health care, research, and medical education: a cross-sectional study. Lancet. 2012 Jul 7;380(9836):37-43. doi: 10.1016/S0140-6736(12)60240-2. Epub 2012 May 10. — View Citation

Chow SK, Wong FK. A randomized controlled trial of a nurse-led case management programme for hospital-discharged older adults with co-morbidities. J Adv Nurs. 2014 Oct;70(10):2257-71. doi: 10.1111/jan.12375. Epub 2014 Mar 12. — View Citation

Conway A, Inglis SC, Chang AM, Horton-Breshears M, Cleland JG, Clark RA. Not all systematic reviews are systematic: a meta-review of the quality of systematic reviews for non-invasive remote monitoring in heart failure. J Telemed Telecare. 2013 Sep;19(6):326-37. doi: 10.1177/1357633X13503427. Epub 2013 Sep 25. Review. — View Citation

Conway A, Inglis SC, Clark RA. Effective technologies for noninvasive remote monitoring in heart failure. Telemed J E Health. 2014 Jun;20(6):531-8. doi: 10.1089/tmj.2013.0267. Epub 2014 Apr 14. Review. — View Citation

Conway G. Case management for heart failure in the emergency department. Crit Pathw Cardiol. 2006 Mar;5(1):25-8. doi: 10.1097/01.hpc.0000202240.99184.81. — View Citation

Cruz J, Brooks D, Marques A. Home telemonitoring effectiveness in COPD: a systematic review. Int J Clin Pract. 2014 Mar;68(3):369-78. doi: 10.1111/ijcp.12345. Epub 2014 Jan 28. Review. — View Citation

Ekeland AG, Bowes A, Flottorp S. Effectiveness of telemedicine: a systematic review of reviews. Int J Med Inform. 2010 Nov;79(11):736-71. doi: 10.1016/j.ijmedinf.2010.08.006. Review. — View Citation

Ekeland AG, Bowes A, Flottorp S. Methodologies for assessing telemedicine: a systematic review of reviews. Int J Med Inform. 2012 Jan;81(1):1-11. doi: 10.1016/j.ijmedinf.2011.10.009. Epub 2011 Nov 21. Review. — View Citation

Elbert NJ, van Os-Medendorp H, van Renselaar W, Ekeland AG, Hakkaart-van Roijen L, Raat H, Nijsten TE, Pasmans SG. Effectiveness and cost-effectiveness of ehealth interventions in somatic diseases: a systematic review of systematic reviews and meta-analyses. J Med Internet Res. 2014 Apr 16;16(4):e110. doi: 10.2196/jmir.2790. Review. — View Citation

Fabbri LM, Boyd C, Boschetto P, Rabe KF, Buist AS, Yawn B, Leff B, Kent DM, Schünemann HJ; ATS/ERS Ad Hoc Committee on Integrating and Coordinating Efforts in COPD Guideline Development.. How to integrate multiple comorbidities in guideline development: article 10 in Integrating and coordinating efforts in COPD guideline development. An official ATS/ERS workshop report. Proc Am Thorac Soc. 2012 Dec;9(5):274-81. doi: 10.1513/pats.201208-063ST. Review. — View Citation

Feltner C, Jones CD, Cené CW, Zheng ZJ, Sueta CA, Coker-Schwimmer EJ, Arvanitis M, Lohr KN, Middleton JC, Jonas DE. Transitional care interventions to prevent readmissions for persons with heart failure: a systematic review and meta-analysis. Ann Intern Med. 2014 Jun 3;160(11):774-84. doi: 10.7326/M14-0083. Review. — View Citation

Goldstein RS, O'Hoski S. Telemedicine in COPD: time to pause. Chest. 2014 May;145(5):945-9. doi: 10.1378/chest.13-1656. Review. — View Citation

Kitsiou S, Paré G, Jaana M. Effects of home telemonitoring interventions on patients with chronic heart failure: an overview of systematic reviews. J Med Internet Res. 2015 Mar 12;17(3):e63. doi: 10.2196/jmir.4174. Review. — View Citation

Kitsiou S, Paré G, Jaana M. Systematic reviews and meta-analyses of home telemonitoring interventions for patients with chronic diseases: a critical assessment of their methodological quality. J Med Internet Res. 2013 Jul 23;15(7):e150. doi: 10.2196/jmir.2770. Review. Erratum in: J Med Internet Res. 2013;15(11):e253. — View Citation

Kotb A, Cameron C, Hsieh S, Wells G. Comparative effectiveness of different forms of telemedicine for individuals with heart failure (HF): a systematic review and network meta-analysis. PLoS One. 2015 Feb 25;10(2):e0118681. doi: 10.1371/journal.pone.0118681. eCollection 2015. Review. — View Citation

Lefèvre T, d'Ivernois JF, De Andrade V, Crozet C, Lombrail P, Gagnayre R. What do we mean by multimorbidity? An analysis of the literature on multimorbidity measures, associated factors, and impact on health services organization. Rev Epidemiol Sante Publique. 2014 Oct;62(5):305-14. doi: 10.1016/j.respe.2014.09.002. Epub 2014 Oct 25. Review. — View Citation

Lundell S, Holmner Å, Rehn B, Nyberg A, Wadell K. Telehealthcare in COPD: a systematic review and meta-analysis on physical outcomes and dyspnea. Respir Med. 2015 Jan;109(1):11-26. doi: 10.1016/j.rmed.2014.10.008. Epub 2014 Oct 27. Review. — View Citation

Marcolino MS, Maia JX, Alkmim MB, Boersma E, Ribeiro AL. Telemedicine application in the care of diabetes patients: systematic review and meta-analysis. PLoS One. 2013 Nov 8;8(11):e79246. doi: 10.1371/journal.pone.0079246. eCollection 2013. — View Citation

Martín-Lesende I, Orruño E, Bilbao A, Vergara I, Cairo MC, Bayón JC, Reviriego E, Romo MI, Larrañaga J, Asua J, Abad R, Recalde E. Impact of telemonitoring home care patients with heart failure or chronic lung disease from primary care on healthcare resource use (the TELBIL study randomised controlled trial). BMC Health Serv Res. 2013 Mar 28;13:118. doi: 10.1186/1472-6963-13-118. — View Citation

Nakamura N, Koga T, Iseki H. A meta-analysis of remote patient monitoring for chronic heart failure patients. J Telemed Telecare. 2014 Jan;20(1):11-7. doi: 10.1177/1357633X13517352. Epub 2013 Dec 18. Review. — View Citation

Onder G, Palmer K, Navickas R, Jureviciene E, Mammarella F, Strandzheva M, Mannucci P, Pecorelli S, Marengoni A; Joint Action on Chronic Diseases and Promoting Healthy Ageing across the Life Cycle (JA-CHRODIS).. Time to face the challenge of multimorbidity. A European perspective from the joint action on chronic diseases and promoting healthy ageing across the life cycle (JA-CHRODIS). Eur J Intern Med. 2015 Apr;26(3):157-9. doi: 10.1016/j.ejim.2015.02.020. Epub 2015 Mar 18. Review. — View Citation

Pandor A, Gomersall T, Stevens JW, Wang J, Al-Mohammad A, Bakhai A, Cleland JG, Cowie MR, Wong R. Remote monitoring after recent hospital discharge in patients with heart failure: a systematic review and network meta-analysis. Heart. 2013 Dec;99(23):1717-26. doi: 10.1136/heartjnl-2013-303811. Epub 2013 May 16. Review. — View Citation

Prochaska JO, DiClemente CC. Transtheorical therapy toward a more integrative model of change. Psychotherapy: Theory, Research and Practice, 1982;19(3):276-287

Purcell R, McInnes S, Halcomb EJ. Telemonitoring can assist in managing cardiovascular disease in primary care: a systematic review of systematic reviews. BMC Fam Pract. 2014 Mar 7;15:43. doi: 10.1186/1471-2296-15-43. Review. — View Citation

Smith SM, Soubhi H, Fortin M, Hudon C, O'Dowd T. Managing patients with multimorbidity: systematic review of interventions in primary care and community settings. BMJ. 2012 Sep 3;345:e5205. doi: 10.1136/bmj.e5205. Review. — View Citation

Sutherland D, Hayter M. Structured review: evaluating the effectiveness of nurse case managers in improving health outcomes in three major chronic diseases. J Clin Nurs. 2009 Nov;18(21):2978-92. doi: 10.1111/j.1365-2702.2009.02900.x. Epub 2009 Sep 11. Review. — View Citation

Wilkinson TM, Donaldson GC, Hurst JR, Seemungal TA, Wedzicha JA. Early therapy improves outcomes of exacerbations of chronic obstructive pulmonary disease. Am J Respir Crit Care Med. 2004 Jun 15;169(12):1298-303. Epub 2004 Feb 27. — View Citation

* Note: There are 27 references in allClick here to view all references

Outcome

Type Measure Description Time frame Safety issue
Primary Sensitivity and specificity of the tele-notifications through study completion, an average of 11 months
Secondary Sensitivity and specificity of the STABILITY SYSTEM INDICATORS through study completion, an average of 11 months
Secondary Specific self-administered questionnaires about Ease of Use/Usefulness/Satisfaction for each category of user through study completion, an average of 11 months
Secondary Acceptability of the system by patients regarding transmission of measured parameters Mean number of transmission of measured parameters: real versus theoretical. through study completion, an average of 11 months
Secondary Acceptability of the system by patients: mean number of participation in virtual classroom session through study completion, an average of 11 months
Secondary Acceptability of the system by patients: mean duration of participation in virtual classroom session through study completion, an average of 11 months
Secondary Acceptability of the system by patients: mean number of consultations of modules providing medical information through study completion, an average of 11 months
Secondary Acceptability of the system by patients: cumulative time spent on consultations of modules providing medical information through study completion, an average of 11 months
Secondary Acceptability of the system by patients: mean duration of phone contacts by type (planned, for notification management, incoming) through study completion, an average of 11 months
Secondary Acceptability of the system by patients: mean number of phone contacts by type (planned, for notification management, incoming) through study completion, an average of 11 months
Secondary Acceptability of the system by patients: comparison of real planned phone contacts versus theoretical through study completion, an average of 11 months
Secondary Acceptability of the system by physicians: mean number of connections through study completion, an average of 11 months
Secondary Acceptability of the system by physicians: mean duration of connections through study completion, an average of 11 months
Secondary Feasibility of the intervention for patients number of screening failure and prematurely withdrawal through study completion, an average of 11 months
Secondary Feasibility of the intervention for technicians duration of intervention through study completion, an average of 11 months
Secondary Feasibility of the intervention for nurses response time following a notification through study completion, an average of 11 months
Secondary Technological performance indices of the system: failures in data transmission through study completion, an average of 11 months
Secondary Technological performance indices of the system: inaccessibility through study completion, an average of 11 months
Secondary Technological performance indices of the system: devices deficiencies technical problems with any medical devices (leading or not to replacement). through study completion, an average of 11 months
Secondary Number of tele-notification per patient through study completion, an average of 11 months
Secondary Frequency of tele-notifications per patient through study completion, an average of 11 months
Secondary Patient care plan: number of changes implemented by investigators. through study completion, an average of 11 months
Secondary Clinical events including medical consultations, hospitalizations and adverse events Overall description of medical consultations, hospitalizations and adverse events. For adverse events, in addition, evaluation of seriousness and causal relationship with the medical device of the study. through study completion, an average of 11 months
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