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Cystic Fibrosis clinical trials

View clinical trials related to Cystic Fibrosis.

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NCT ID: NCT04825236 Completed - Cystic Fibrosis Clinical Trials

MyVoice:CF Decision Aid for Women With Cystic Fibrosis

Start date: July 1, 2021
Phase: N/A
Study type: Interventional

This project is a single-center feasibility study of MyVoice:CF, a patient-facing, web-based decision aid. Aim 1) Assess the acceptability, feasibility, and usability of MyVoice:CF for women with CF and multidisciplinary adult CF providers. Aim 2) Assess the preliminary efficacy of MyVoice:CF related to patient-provider communication, shared decision-making, knowledge, and self-efficacy for women with CF related to reproductive health concerns.

NCT ID: NCT04809207 Completed - Cystic Fibrosis Clinical Trials

Acceptability, Feasibility and Preliminary Efficacy of CFWP to Treat Clinically Elevated Fatigue in Adults With CF

Start date: May 1, 2021
Phase: N/A
Study type: Interventional

This research is being done to learn more ways to treat non-respiratory symptoms in people with CF including fatigue, pain, mood, sleep problems and the use of a wellness program to treat them.

NCT ID: NCT04803643 Completed - Cystic Fibrosis Clinical Trials

Upper Extremity Exercise Capacity, Muscle Oxygenation, Balance in Patients With Cystic Fibrosis

Start date: March 16, 2021
Phase:
Study type: Observational

The primary aim of the study is to evaluate upper extremity exercise capacity, muscle oxygenation, balance and physical activity level in patients with cystic fibrosis.. The secondary aim of the study is assessment of functional exercise capacity, respiratory function, peripheral and respiratory muscle strength, respiratory muscle endurance, quality of life in patients with cystic fibrosis and compare them with healthy controls.

NCT ID: NCT04798014 Completed - Cystic Fibrosis Clinical Trials

HERO-2: Home-Reported Outcomes With CFTR Modulator Therapy

Start date: May 26, 2021
Phase:
Study type: Observational

This is an observational cohort study, using data from Folia Health and the Cystic Fibrosis Foundation Patient Registry (CFFPR). Individuals taking elexacaftor/tezacaftor/ivacaftor (ETI) may be enrolled through the Folia application. During the 12-month study period, participants will be asked to track their routine treatment and medication usage, daily symptoms, and monthly review with validated patient-reported outcome (PRO) questionnaires. Participants will also be asked to self-report instances of changes to their treatment plan, and pulmonary exacerbations. There are no study-associated site visits.

NCT ID: NCT04777344 Completed - Cystic Fibrosis Clinical Trials

Clinical Effort Against Smoke Exposure in Cystic Fibrosis

CEASE-CF
Start date: July 8, 2021
Phase: N/A
Study type: Interventional

The study will test the feasibility, acceptability, and preliminary efficacy of a multi-component smoking cessation intervention tailored to the needs of caregivers of children with CF and delivered in clinical settings as part of routine CF care. The ultimate goal of this effort is to reduce the exposure of children and adolescents with CF to tobacco smoke.

NCT ID: NCT04743206 Completed - Cystic Fibrosis Clinical Trials

Airway Clearance for Pediatric and Adult Cystic Fibrosis Patients Using a Portable Intra-Pulmonary Percussion Device

Start date: May 18, 2021
Phase: N/A
Study type: Interventional

This is a pilot study where the investigators aim to compare initial use of the standard airway clearance device (SACD), most commonly used being High frequency vest airway clearance system (VEST) with subsequent use of a Portable Intra-Pulmonary Percussion Device (PIAPD) in patients with cystic fibrosis (CF) ages 6 -21 years. The primary hypothesis is that there is no effect of PIAPD on Forced expiratory volume in 1 second (FEV1) 2 hours after use, there is no effect on perception of effort and efficacy for the PIAPD. If both are equally effective, the latter device provides an alternative that is both cheaper and portable.

NCT ID: NCT04742049 Completed - Covid19 Clinical Trials

The Effects of Telerehabilitation on Muscle Function, Physical Activity and Sleep in Cystic Fibrosis During Pandemic

Start date: December 28, 2020
Phase: N/A
Study type: Interventional

The aim of this study is to evaluate the peripheral muscle function, sleep disorders and physical activity level in children with cystic fibrosis who are physically inactive at home due to social isolation and to examine the effect of the 6-week online exercise protocol.

NCT ID: NCT04734743 Completed - Cystic Fibrosis Clinical Trials

Muscle Strength, Functional Capacity, Respiratory Function and Quality Of Life In Cystic Fibrosis Patients

Start date: May 1, 2016
Phase: N/A
Study type: Interventional

This study was designed to investigate the relationship between upper extremity muscle strength and endurance, functional capacity, and quality of life child and adolescent with cystic fibrosis

NCT ID: NCT04732195 Completed - Cystic Fibrosis Clinical Trials

Pilocarpine Microneedles for Sweat Induction (PMN-SI)

Start date: January 20, 2022
Phase: N/A
Study type: Interventional

The investigators want to test in this non-randomized clinical trial a new method of administrating Pilocarpine medicine into the skin during the Sweat testing process that does not use any electrical current.

NCT ID: NCT04702386 Completed - Cystic Fibrosis Clinical Trials

Concerns of Children Whose Parents Have Cystic Fibrosis

MUCOKIDS
Start date: February 18, 2021
Phase:
Study type: Observational

As more and more patients with cystic fibrosis (CF) become parents, we have studied parenting concerns in this serious chronic disease in a first study (MucoPar) which is ongoing. The current study (MucoKids) is an extension of the previous MucoPar study and aims to explore and collect the perceptions, expectations and needs of children whose one parent has CF. This will be done in the context of individual interviews or in several small groups of children led by a psychologist who will encourage them to develop what constitutes to be the child of somebody with CF. The collected information should make it possible to develop and propose adapted medico-psycho-social interventions, if necessary, in connection with patient associations.