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Study of Satisfaction of Patients and Care Providers for an Alternate Follow-up With In-hospital Consults and Tele-consult for Patients With Cystic Fibrosis

FollowMuco : Study of Satisfaction of Patients and Care Providers for an Alternate Follow-up With In-hospital Consults and Tele-consult for Patients With Cystic Fibrosis

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05249322
Acronym
FollowMuco
Enrollment
30
Registered
2022-02-21
Start date
2022-03-31
Completion date
2024-03-31
Last updated
2023-09-28

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

Conditions

Cystic Fibrosis

Keywords

tele-medicine, cystic fibrosis, alternate follow-up

Brief summary

The pandemic forced us to develop home follow-up for patients with chronical diseases . In the same time, the new era of treatment for cystic fibrosis considerably improves the health of patients with this pathology. This study aims to assess the satisfaction of patients and care providers for an alternated follow-up between tele-consults and in-hospital consults during one year for patients with cystic fibrosis treated by Kaftrio® since at least one year and stable.

Interventions

OTHERFollow-up alternating between face-to-face consultation and teleconsultation every three months.

The intervention will be an alternate follow-up every three months with: * A tele-consult: with paramedical consult (with assistance for home-spirometry) and medical consult for about 1h30 in total, make with a HCL platform for telemedicine. * An usual in-hospital consult of about 1h30 with paramedical and medical consult.

Sponsors

Hospices Civils de Lyon
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

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

Inclusion criteria

* patients with cystic fibrosis * Patients treated with Kaftrio® since one year * autonomous patients * patients without cognitive disorders * Patients voluntary for this follow up * patients with two tele-communication tools * patients with FEV1\>50% * patients with less of 2 antibiotics cure per year

Exclusion criteria

* all transplanted patients * Pregnant patients * Particular follow up needed in-hospital consult * Persons deprived of their liberty by a judicial or administrative decision * Persons subject to psychiatric care * Persons admitted to a health or social establishment for purposes other than research * Persons not affiliated to a social security scheme or beneficiaries of a similar scheme

Design outcomes

Primary

MeasureTime frameDescription
Change in Patients and care providers satisfaction after one year of alternated follow-up (hospital Consults and Tele-consult)Measured at inclusion and after one year of follow up.Satisfaction of patients and care providers for the follow-up by the Client-Satisfaction-Questionnaire (CSQ-8 for patients and CSQ-3 for care-provider). For the CSQ-8 the minimum value is 8 and the maximum value is 32. There is three levels: Low satisfaction (8-20), medium satisfaction (21-26) and high satisfaction (27-32) .

Secondary

MeasureTime frameDescription
Comparison between FEV1 measured at the department's respiratory functional exploration center and FEV1 measured with the Spirobank ® during the same in-hospital visit.At inclusion, 6month and 12 monthComparison between FEV1 measured at the department's respiratory functional exploration center and FEV1 measured with the Spirobank ® during the same in-hospital visit in order to check that the difference between the two values does not exceed the margin of error of 5%.
effect on Patients and care providers quality of lifeMeasured at inclusion and after one yearQuality of life of patients by Cystic fibrosis questionnaire revised(CFQ-R). The CFQ-R is a validated patient-reported outcome measuring health-related quality of life for children and adults with CF. The CFQ-R contains both general and CF-specific scales. The CFQ-R was administered at Days 0, 14, 28, and 42. The endpoint was change in respiratory symptoms (e.g., coughing, congestion, wheezing) from Day 0 (baseline), assessed with the CFQ-R RSS (score range: 0-100; higher scores indicating fewer symptoms, higher health-related quality of life, or better functioning). Baseline CFQ-R RSS and age group (\<18 vs. \>=18 years) were included as covariates in the analysis.
effect on Patients FEV1 (Forced expiratory volume)Measured at inclusion and after one yearFEV1 measured in start and at the end of the study
Patients and care providers satisfaction for tele consultationMeasured after tele-consult (at 6 month M+6 and at 12 month M+12)Satisfaction of patients and care providers for tele-consults by telemedicine satisfaction Questionnaire (TSQ). The TSQ is a 14-item questionnaire in its final version, the questionnaire items are scored on a five-point scale, from 1 being strongly disagree to 5 being strongly agree.. The internal consistency of the TSQ was 0.93, which is considered acceptable and indicates strong correlations between the items that make up the scale. Predictive validity supported the conclusion that the TSQ measured patient satisfaction with telemedicine (Pearson's correlation coefficient (r=0.45, P\<0.05).
effect on patient's weightMeasured at inclusion and after one yearWeight measured in start and at the end of the study
Effect on Patients call and mail to CF centerMeasured at inclusion and after one yearNumber of calls and mails to CF center during one year before start and after one year of the study
effect on Patients antibiotic cure numberMeasured at inclusion and after one yearAntibiotic cure during one year before start and after one year of the study

Countries

France

Contacts

Primary ContactThomas VIDAL
Thomas.vidal@chu-lyon.fr478865671
Backup ContactIsabelle Durieu, Pr
isabelle.durieu@chu-lyon.fr

Outcome results

None listed

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