Investigating a Well-being Review in Pulmonary Hypertension
NCT ID: NCT04840251
Last Updated: 2021-04-09
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
WITHDRAWN
NA
INTERVENTIONAL
2021-03-31
2023-05-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Aim: To see if it is feasible to study physiotherapy well-being reviews in PH. Step 1: We will interview some patients with PH who have had rehabilitation and ask questions about their experiences. We will also ask what they think we should measure to show any difference their rehabilitation has made to them. The findings from Step 1 will help us to shape the details of Step 2, where we will conduct a small study to see if it is feasible to run a full study. Participants will be divided randomly into a treatment group and a control group. The treatment group will have a physiotherapy well-being review, leading to referral to their most suitable local rehabilitation service and follow-up after 6 months. The control group will receive brief exercise advice and follow-up after 6 months. The findings will help to design a full study and be shared with patients and health professionals.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Exercise-based Rehabilitation in Patients With Pulmonary Arterial Hypertension
NCT06804122
Rehabilitation for Patients With Pulmonary Arterial Hypertension
NCT00544726
Effects of Pulmonary Rehabilitation on Quality of Life and Health in Pulmonary Arterial Hypertension Patients
NCT06973382
Home Rehabilitation Improves Cardiac Effort in Pulmonary Arterial Hypertension
NCT06477640
Rehabilitation for Patients With Pulmonary Hypertension
NCT03955016
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Intervention
The treatment group will have a physiotherapy well-being review and be referred for rehabilitation. They will be seen after 6 months for follow-up
Well-being review and rehabiliation
For their well-being review, patients will meet with a physiotherapist specialist in PH and discuss:
* how they are
* what they can do for themselves
* what it is challenging for them to do
* how active they are
* if they have ever exercised before The physiotherapist will then make a referral to the most suitable rehabilitation service local to the patient e.g. rehabilitation classes, physiotherapy at home, weight-loss programmes.
Control
The control group will have initial assessments then receive brief advice on exercise. They will also be followed up after 6 months
No interventions assigned to this group
Qualitative
to understand how it feels to take part in the well-being review, we will interview some participants who have already had this kind of treatment and ask questions about their experiences of it and how it was for them. We are also interested to know what differences they felt it made so that we can help to decide about the things we want to measure as outcomes in the interventional of the study.
Qualitative Interviews
Patients who have previously undergone rehabilitation will take part in a semi-structured interview to explore their experience and the impact it has had
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Well-being review and rehabiliation
For their well-being review, patients will meet with a physiotherapist specialist in PH and discuss:
* how they are
* what they can do for themselves
* what it is challenging for them to do
* how active they are
* if they have ever exercised before The physiotherapist will then make a referral to the most suitable rehabilitation service local to the patient e.g. rehabilitation classes, physiotherapy at home, weight-loss programmes.
Qualitative Interviews
Patients who have previously undergone rehabilitation will take part in a semi-structured interview to explore their experience and the impact it has had
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* have a diagnosis of PH
* have started on PH drug therapy in the preceding 18 months
* showing no signs of worsening breathlessness or heart failure
* on an unchanged PH therapeutic regime for at least 6 months prior to inclusion.
Exclusion Criteria
* have participated in a clinical study involving another investigation of drug, device or exercise within the previous 6 months
* are on a surgical or other pathway of care that has pre-determined physiotherapy or activity regimes or restrictions
* have any additional medical conditions that may adversely affect the safety of the subject or severely limit the lifespan of the subject
* have participated in rehabilitation in the last 12 months.
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Sheffield Teaching Hospitals NHS Foundation Trust
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Sheffield Teaching Sospitals NHS Foundation Trust
Sheffield, , United Kingdom
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
STH20898
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.