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Development,Effectiveness and Cost-effectiveness of a New Respiratory and Palliative Care Out-patient Breathlessness Support Service


Phase 3
16 Years
90 Years
Open (Enrolling)
Both
Breathless Patients With Any Established Underlying Medical Diagnosis

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Trial Information

Development,Effectiveness and Cost-effectiveness of a New Respiratory and Palliative Care Out-patient Breathlessness Support Service


Inclusion Criteria:



- Patients with any established underlying medical diagnosis with breathlessness on
exertion or at rest.

- Cancer patients who have risk factors for breathlessness( risk factors include a
history of smoking, asthma or COPD, lung irradiation, exposure to asbestos, coal
dust, cotton dust or grain dust, lung involvement by cancer)

- Respiratory muscle weakness

- Anxiety.

- Patients must have advanced disease that is refractory to maximal optimised medical
management. - Patients must be able to engage with a short term physiotherapy and
occupational therapy intervention.

Exclusion Criteria:

- Patients with breathlessness of unknown cause.

- Chronic hyperventilation syndrome.

Type of Study:

Interventional

Study Design:

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Health Services Research

Outcome Measure:

Chronic Respiratory Disease Questionnaire (CRQ)

Outcome Description:

The primary outcome measure will be improvement of mastery of breathlessness, as assessed by a change in the score within the Mastery domain of the chronic respiratory disease questionnaire (CRQ).

Outcome Time Frame:

12 weeks

Safety Issue:

No

Principal Investigator

John Moxham, MD FRCP

Investigator Role:

Study Director

Investigator Affiliation:

King's College London

Authority:

United Kingdom: National Health Service

Study ID:

10/H0808/17

NCT ID:

NCT01165034

Start Date:

July 2010

Completion Date:

May 2013

Related Keywords:

  • Breathless Patients With Any Established Underlying Medical Diagnosis
  • Dyspnea

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