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Completed

NCT Number: NCT04172155

Pulmonary Rehabilitation and Self-esteem in Patients With COPD

the aim of this study is to evaluate the evolution of self-esteem during a pulmonary rehabilitation program, in COPD patients.

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Key information

Conditions

COPD Chronic Disease Disease Attributes Lung Diseases Lung Diseases, Obstructive Pathologic Processes Pathological Conditions, Signs and Symptoms Pulmonary Disease, Chronic Obstructive Respiratory Tract Diseases

Age range

18 year–90 year

Sex eligibility

All sexes

Study type

Observational

Primary location

CHRU de Brest, Brest, France

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patient with stage 2 to 4 (A to D) COPD admitted to a pulmonary rehabilitation program
  • Patient aged 18 or over
  • Patient able to consent and having signed a consent form

Exclusion criteria

  • Patient with pain, osteoarthritis or shoulder surgery
  • Patient with a history of Pneumonectomy, lobectomy less than 6 months old
  • Refusal of participation
  • Patient with an inability to complete a pulmonary rehabilitation program in totality
  • Pregnant or breast-feeding women
  • Patient under tutorship or curatorship

Treatment and study plan

Primary outcomes

  1. PSI-6

    Time frame: PSI-6 is measured at the biginning and at the end of the pulmonary rehabilitation program (4 weeks)

    the physical self inventory- 6 (PSI-6) allows to evaluate self esteem

Secondary outcomes

  1. 6MWT

    Time frame: the 6MWT is measured at the biginning and at the end of the pulmonary rehabilitation program (4 weeks)

    The 6-minute walk test allows to evaluate exercise capacity

  2. HAD

    Time frame: HAD is measured at the biginning and at the end of the pulmonary rehabilitation program (4 weeks)

    the hospital anxiety and depressive scale (HAD) measure the anxiety and depression

  3. SGRQ

    Time frame: SGRQ is measured at the biginning and at the end of the pulmonary rehabilitation program (4 weeks)

    the Saint-George respiratory Questionnaire (SGRQ) measure the quality of life

Other outcomes

  1. MMRC

    Time frame: MMRC is measured at the biginning and at the end of the pulmonary rehabilitation program (4 weeks)

    The modified medical research Council dyspnea scale measure dyspnea

Sponsors and collaborators

Lead sponsor

University Hospital, Brest

Other

Registry information

Official study title

Effects of Pulmonary Rehabilitation on Self-esteem in Patients With COPD

Acronym: ESMOI

Important dates

Study start
2019
Primary completion
2020
Study completion
2020
First posted
Nov 21, 2019
Registry last updated
Jan 27, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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