Cognitive-behavioral Treatment for Rheumatoid Arthritis
NCT ID: NCT02257073
Last Updated: 2017-04-04
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
UNKNOWN
NA
150 participants
INTERVENTIONAL
2014-10-31
2020-07-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Cognitive-Behavioral Therapy and Tai Chi Chih for Patients With Rheumatoid Arthritis
NCT00072657
Relaxation Response Training for the Treatment of Rheumatoid Arthritis
NCT00056667
Effects of a Rheumatoid Arthritis Self-management Program
NCT03470740
Anxiety Depression and Rheumatoid Arthritis
NCT03061877
Pain and Stress Management for People With Rheumatoid Arthritis
NCT00088764
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
TREATMENT
SINGLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
CBT
Cognitive-behavioral treatment
Cognitive-behavioral treatment
WLT
Waiting in list
Waiting List
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Cognitive-behavioral treatment
Waiting List
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
Exclusion Criteria
* currently receiving mental health care
* any medical condition that might prevent them from safely exercising (e.g. history of more severe heart, lung or cerebrovascular disease)
* previously attended an education programme
* had a Modified Health Assessment Questionnaire score \>2 (score range 0-3), that is severe functional problems
* history of organic brain syndrome
* presence of a psychotic disorder
* presence of other uncontrolled medical disorders
* presence of a major communication disorder, illiteracy
* presence of less than an 8th grade education (due to inability to complete questionnaires)
* presence of a therapeutic dosage of an antidepressant medication, or presence of another autoimmune disease/disabling condition
18 Years
75 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Chengdu PLA General Hospital
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Yang Min
Dr.
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
General Hospital of Chengdu Military Area Command PLA
Chengdu, Sichuan, China
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
BWS11J067
Identifier Type: OTHER_GRANT
Identifier Source: secondary_id
CBRA20140102
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.