Study on Pulmonary Rehabilitation for Stable Chronic Obstructive Pulmonary Disease(COPD) Patients

NCT ID: NCT04741373

Last Updated: 2021-04-13

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: NA
• Total Enrollment: 90 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2021-04-01
• Study Completion Date: 2021-09-01

Brief Summary

To compare the difference of effectiveness for stable COPD patients with poor nutritional status among three groups named health education, upper and lower limb exercises, and oral nutritional supplements. Then formulate the best pulmonary rehabilitation guidance strategy according to the result of this trial.

Detailed Description

This study is a clinical randomized, non-blinded, controlled study in China. The participants will be 90 stable COPD patients with poor nutritional status selected by the community or primary hospitals. On the principle of having no statistical difference in indicators such as baseline age, Global Initiative for Chronic Obstructive Lung Disease（GOLD） staging, and medication oxygen consumption among the groups , the trial will randomly be divided into three groups: health education group, health education + upper and lower extremity exercise group, health education + upper and lower extremity exercise + oral nutritional supplements group.

A 12-week pulmonary rehabilitation clinical study will be conducted to observe the difference of outcome indicators among the three groups like nutritional status (24hr diet, body weight, body composition, albumin), pulmonary function (classification and staging), muscle strength and muscular endurance (grip strength, 6-minute walking distance(6MWD)), inflammation factors and St. George's Respiratory Questionnaire (SGRQ) score. Moreover outcome indicators after 24 weeks like patient weight, SGRQ score and GOLD staging also will be recorded for comparison.

The project will evidence-based provide effective means like nutrition and exercise for Chinese malnourished COPD patients who are at stable stage. And popular science books on pulmonary rehabilitation based on this trial will be compiled to record the best pulmonary rehabilitation guidance strategies.

Conditions

Nutritional Support; Aerobic Exercise; Respiratory Function Tests; Body Composition; Muscle Strength

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Group of health education

Group Type: PLACEBO_COMPARATOR

health education

Intervention Type: OTHER

Establish WeChat group or QQ group or telephone contact, and regularly distribute electronic science pictures or small videos

Group of health education and rehabilitation exercise

Group Type: ACTIVE_COMPARATOR

rehabilitation exercise

Intervention Type: BEHAVIORAL

Aerobic exercise: fixed cycling in rehabilitation center or walking at home, 3-5 times/week, Resistance exercise: lift dumbbell by upper limb, raise legs tying sandbags, 2-3 times/week

health education

Intervention Type: OTHER

Establish WeChat group or QQ group or telephone contact, and regularly distribute electronic science pictures or small videos

Group of health education,exercise and ONS

Group Type: EXPERIMENTAL

oral nutritional supplements

Intervention Type: DIETARY_SUPPLEMENT

oral nutritional supplements, 400-600kcal/day;

rehabilitation exercise

Intervention Type: BEHAVIORAL

Aerobic exercise: fixed cycling in rehabilitation center or walking at home, 3-5 times/week, Resistance exercise: lift dumbbell by upper limb, raise legs tying sandbags, 2-3 times/week

health education

Intervention Type: OTHER

Establish WeChat group or QQ group or telephone contact, and regularly distribute electronic science pictures or small videos

Interventions

oral nutritional supplements

oral nutritional supplements, 400-600kcal/day;

Intervention Type: DIETARY_SUPPLEMENT

rehabilitation exercise

Aerobic exercise: fixed cycling in rehabilitation center or walking at home, 3-5 times/week, Resistance exercise: lift dumbbell by upper limb, raise legs tying sandbags, 2-3 times/week

Intervention Type: BEHAVIORAL

health education

Establish WeChat group or QQ group or telephone contact, and regularly distribute electronic science pictures or small videos

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

1. Patients with moderate and severe COPD with a clear diagnosis of lung function, (moderate-forced expiratory volume at one second（FEV1）/forced vital capacity（FVC）<0.7, FEV1% between 50-80%; severe-FEV1/FVC<0.7, FEV1% < 50%).

2. Patients are at stable stage of COPD which means hospital admission <2 times due to acute exacerbation in the past two years, no changes in respiratory symptoms and medication in the past month.

3. Patients have not participated in any form of pulmonary rehabilitation in the past at least 0.5 year and simultaneously have not taken any form of nutritional supplements in the past at least 2 weeks.

4. Malnutrition criteria: Mini Nutritional Assessment-ShortForm(MNA-SF) ≤ 12 points; or Body Mass Index(BMI) ≤ 21kg/m2.

5. Volunteers have the ability to complete the test of lung function, grip strength, 6MWD, body composition and blood index tests.

Exclusion Criteria

1. Patients suffer from significant diseases which will cause the subjects to be at risk due to participating in the research, or affect the research results and the subjects' ability to participate in the research,including severe diseases of liver and kidney, nervous system, endocrine and digestive system .

2. Patients have ischemic heart disease with a history of angina pectoris, or uncontrolled chest tightness and angina pectoris after activities recently.

3. Patients have severe pulmonary hypertension or grade IV by heart function grade of New York Heart Association(NYHA).

4. Arterial oxygen saturation (SpO2) <88% or PaCO2> 55mmHg in a quiet state.

5. Those whose life cycle is expected to be less than 6 months.

6. Walking restriction is limited in 300m because of intermittent claudication caused by peripheral arterial disease or osteoporosis.

7. Patients lost capability of autonomous activity or have cognitive impairment.

• Minimum Eligible Age: 40 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Fudan University

OTHER

Sponsor Role: lead

Responsible Party

Zhijun Bao

Director

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Jie Chen, PhD

Role: STUDY_DIRECTOR

Huadong Hospital

Locations

Huadong Hospital Affiliated to Fudan University

Shanghai, , China

Site Status: RECRUITING

Countries

China

Central Contacts

Min Zong, MD

Role: CONTACT

zmmlily@163.com

+86 13524018935

Facility Contacts

Jiang Wu, PhD

Role: primary

Other Identifiers

Huadong Hospital to Fudan

Identifier Type: -

Identifier Source: org_study_id