- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02198989
Effects of Peer Support and Yoga Music on T2DM With Depression and Sleep Disorders
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Research Method:
This study is an open- label controlled randomized cluster trial with the sample size estimated by the improvement of Pittsburgh Sleep Quality Index(PSQI) score. 40 eligible and voluntary Type 2 diabetic patients will be recruited among the patients with health records in the community. Baseline assessment such as demography, sleep quality, depression, physical exam and biochemical index will be performed on the patients who will have signed the informed consents.
The study will use the method of randomized to classify the enrolled units into 2 groups, each group has 20 people. Both groups will receive regular diabetes medication and group education courses including Diabetes Self-management Education(DSME), psychological support, improvement in sleep. The intervention group will be under the guidance of two well-trained peer supporters to carry out group activities. Each supporter will be in charge of 10-15 patients. Starting with peer support therapy in the first three months, the intervention group will then take Yoga music therapy before bed for another three months and be given support and guidance by the peer supporters.
Compare the baselines and variations of two group's sleep, depression, blood sugar and related biochemical indicators, and self-management, life quality, medication and other aspects at the third month and sixth month. The final evaluation will show the effect and related influencing factors of peer support and yoga music therapy in helping Type 2 diabetic patients who have sleep disorders and mild depression to improve their sleep quality.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
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Shanghai
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Shanghai, Shanghai, China
- Shanghai Jiao Tong University of Medicine
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-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Confirmed type 2 diabetes patients (ICD9) according to the medical record and patient's disease history
- Diagnosis type 2 diabetes more than 6 months
- 40 Years to 84 Years old
- Sleep-disordered patients (PSQI scores≥7)
- Mild depression condition(14 ≥PHQ-9 scores≥ 5 分)
- Have a stable T2DM condition,without any other diseases affect patients' sleep
- Agree to participate in the study and have signed the Inform Consent Form
Exclusion Criteria:
- Terminal illnes
- Hearing loss or severe visual disorder
- Life expectancy is less than 12 months
- Primary sleep apnoea syndrome
- Serious physical pain that affect the quality of sleep
- Using drugs that affect the quality of sleep
- Individuals with histories of Alcohol or Drug Abuse
- Patients with high risk for sleep apnea syndrome(STOP scores ≥3 )
- Planned to receive selective surgery within 3months
- Observed mental confusion suggesting dementia
- Ongoing psychiatric care
- Paralysis or residence in a long-term care facility
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: peer support and yoga music therapy
Patients in the group will receive peer support and yoga music therapy before bed. Patients in the group will received the group education courses and clinical medical therapy. |
Patients in the intervention group will receive peer support and yoga music therapy before bed.
|
|
No Intervention: Control group
Patients in the group will received the group education courses and clinical medical therapy.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Score on Pittsburgh Sleep Quality Index(PSQI)
Time Frame: 9 months
|
9 months
|
|
Score on Patient Health Questionnaire (PHQ-9)
Time Frame: 9 month
|
9 month
|
|
HbA1c
Time Frame: 9 months
|
9 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
BMI
Time Frame: 9 months
|
9 months
|
|
|
Insulin resistance measured as HOMA-IR
Time Frame: 9 months
|
HOMA-IR = (FINS×FPG) / 22.5
|
9 months
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Study Chair: Liebin Zhao, MSM, Center of Diabetes, Ruijin Hospital, Shanghai Jiao Tong University of Medicine
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- CCEMD-022
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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