Evaluation, Psychological Intervention and Follow-up Study of Anxiety and Depression in Stable COPD Patients

NCT ID: NCT02413840

Last Updated: 2015-04-10

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Clinical Phase

NA

Total Enrollment

60 participants

Study Classification

INTERVENTIONAL

Study Start Date

2014-12-31

Brief Summary

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This study expect to investigate psychological intervention (Baduanjin qigong) in COPD patients combined with anxiety and/or depression.

Detailed Description

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Anxiety and depression is one of the most common complications of COPD patients.This research use psychological questionnaires to evaluate the stage of COPD patients with anxiety and/or depression(asymptomatic, subclinical,clinical). The subclinical type will divided into the treatment group of Baduanjin qigong,and the control group. Two groups are all receive the same psychological counseling, the treatment group also receive further treatment of Baduanjin qigong under the guidance of medical staff. The treatment along for 1 year. Two groups were followed up for 2 years, dynamically observe the stage of anxiety and depression,the number of exacerbations,lung function,etc.

Conditions

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COPD Anxiety Depression

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Baduanjin qigong group

Doing exercise of Baduanjin qigong under the guidance of medical staff;psychological counseling at the same time.

Group Type EXPERIMENTAL

Baduanjin qigong

Intervention Type BEHAVIORAL

control group

Psychological counseling only.

Group Type NO_INTERVENTION

No interventions assigned to this group

Interventions

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Baduanjin qigong

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

* Diagnosed of COPD
* In stable phase
* FEV1%predicted \<80.

Exclusion Criteria

* Cancer
* Severe cerebrovascular disease
* Severe arrhythmia,cardiac insufficiency
* Alzheimer's disease
* Mental illness
* Severe liver disfunction
* Severe renal disfunction
* Physical activity disable.
Minimum Eligible Age

40 Years

Maximum Eligible Age

75 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Huimin Gong

OTHER

Sponsor Role lead

Responsible Party

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Huimin Gong

Resident

Responsibility Role SPONSOR_INVESTIGATOR

Principal Investigators

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Ting Yang

Role: STUDY_CHAIR

Capital Medical University

Locations

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Beijing institute of respiratory diseases

Beijing, , China

Site Status RECRUITING

Countries

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China

Central Contacts

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Huimin Gong

Role: CONTACT

8613436379130

Facility Contacts

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Ting Yang

Role: primary

8613651380809

Other Identifiers

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CMU900314

Identifier Type: -

Identifier Source: org_study_id

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