Effect of Progressive Muscle Relaxation Technique of Fatigue and Quality of Sleep in Pations

Effect of Progressive Muscle Relaxation Technique of Fatigue and Quality of Sleep in Pations with Chronic Obstructive Pulmonary Disease

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

IRCT

Registry ID

IRCT2016080124080N3

Enrollment

100

Registered

2017-03-11

Start date

2016-09-22

Completion date

Unknown

Last updated

2018-02-22

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

Conditions

Chronic Obstructive Pulmonary Disease. Chronic Obstructive Pulmonary Disease, unspecified

Interventions

Intervention 1: for patients in the intervention group will perform Progressive muscle relaxation program.steps of progressive relaxation exercises include Breathing Exercises? lower extremity exerci

Rehabilitation

Treatment - Drugs

for patients in the intervention group will perform Progressive muscle relaxation program.steps of progressive relaxation exercises include Breathing Exercises? lower extremity exercises ?upper extre

Also in the control group they will receive usual care

Eligibility

Sex/Gender

All

Age

45 Years to 75 Years

Inclusion criteria

Inclusion criteria: The inclusion criteria includ: COPD Diagnosed by a physician of at least duration of 6 months or longer; residence in the city; patients with stage 3 or 4 COPD (according to the GOLD system, 2007); absence of a disease diagnosis additional to COPD; ability to read and write and willingness to collaborate ; Having degrees of moderate to severe fatigue and sleep disturbance; based on questionnaire of fatigue and sleep quality index; The absence of disease of the nervous system ? Acute myocardial Infarction And Cancer In addition to copd; Age 45 to 70 years?BMI less than 30 ; Lack of psychiatric disorders such as anxiety . The exclusion criteria include: cognitive disorders;viral infections; participation in pulmonary rehabilitation

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

Measure	Time frame
Fatigue. Timepoint: Immediately before intervention and 8 week after intervention. Method of measurement: Fatigue severity scale(fss).	—

Secondary

Measure	Time frame
Quality of sleep. Timepoint: Immediately before intervention and 8 week after intervention. Method of measurement: Pittsburgh Sleep Quality Index (PSQI).	—

Countries

Iran (Islamic Republic of)

Contacts

Public ContactPooya.Seydi Chegeni

Lorestan University Of Medical Sciences

pooya.seyedi22@gmail.com+98 66 3314 0120

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Mar 7, 2026