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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02746679
Other study ID # MBSR-5
Secondary ID
Status Completed
Phase N/A
First received April 19, 2016
Last updated April 19, 2016
Start date January 2015
Est. completion date January 2016

Study information

Verified date April 2016
Source First Affiliated Hospital, Sun Yat-Sen University
Contact n/a
Is FDA regulated No
Health authority China: Health and Family Planning Commission of Guangdong Province
Study type Interventional

Clinical Trial Summary

The purpose of this study is to determine whether mindfulness based stress reduction are effective on improve anxiety, depression and quality of life in women with intrauterine adhesion


Description:

This is a parallel arm, randomized controlled trials, according to 1: 1 ratio assigned intrauterine adhesions patients to mindfulness based stress reduction group and wait-list control group.The study compared anxiety and depression levels and quality of life in patients with intrauterine adhesions before and after the completion of mindfulness based stress reduction program.Anxiety, depression and quality of life level measured by the Zung self-rating anxiety scale, Zung Self-Rating Depression Scale and The 36-item Short-Form Health Survey.


Recruitment information / eligibility

Status Completed
Enrollment 226
Est. completion date January 2016
Est. primary completion date November 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 20 Years to 46 Years
Eligibility Inclusion Criteria:

1. Meet intrauterine adhesions diagnostic criteria of ESGE.

2. Patients with clear consciousness, can correct understanding related content of the questionnaire.

Exclusion Criteria:

1. Have a history of mental illness.

2. Receiving psychological treatment currently.

3. Have acute mental disorders.

4. Experienced special stress life events within six months.

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Prevention


Related Conditions & MeSH terms


Intervention

Other:
Mindfulness Based Stress Reduction
Mindfulness Based Stress Reduction programs have been shown to be effective, however, the potential benefits of Mindfulness Based Stress Reduction to decrease depression, anxiety, stress in other diseases. Therefore, the purpose of this study was to examine whether MBSR is effective, and has potential as an intervention to decrease depression, anxiety ,and to improve quality of life of intrauterine adhesion patients.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Yuqing Chen

References & Publications (2)

Roth B, Robbins D. Mindfulness-based stress reduction and health-related quality of life: findings from a bilingual inner-city patient population. Psychosom Med. 2004 Jan-Feb;66(1):113-23. — View Citation

Würtzen H, Dalton SO, Elsass P, Sumbundu AD, Steding-Jensen M, Karlsen RV, Andersen KK, Flyger HL, Pedersen AE, Johansen C. Mindfulness significantly reduces self-reported levels of anxiety and depression: results of a randomised controlled trial among 336 Danish women treated for stage I-III breast cancer. Eur J Cancer. 2013 Apr;49(6):1365-73. doi: 10.1016/j.ejca.2012.10.030. Epub 2012 Dec 19. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary The Zung Self-Rating Anxiety Scale scores before and after the intervention 8 weeks No
Secondary Endometrial thickness were measured by ultrasound in the middle of menstruation in all patients. 3 months No
Secondary Menstruation was evaluated with visual analogue scale (VAS) in which the menstruation was assessed by the patients themselves with 0 as amenorrhea and 100 as normal menstruation 3 months No
Secondary The numbers of reformation of intrauterine adhesions were counted by the follow-up hysteroscopy was performed in the third month after the surgery 3 months No
Secondary The Zung Self-Rating Depression Scale scores before and after the intervention 8weeks No
Secondary The scores of physical function before and after the intervention(one dimensions of the 36-item short-form health survey) 8weeks No
Secondary The scores of role-physical before and after the intervention(one dimensions of the 36-item short-form health survey) 8weeks No
Secondary The scores of role-emotional before and after the intervention(one dimensions of the 36-item short-form health survey) 8weeks No
Secondary The scores of vitality before and after the intervention(one dimensions of the 36-item short-form health survey) 8weeks No
Secondary The scores of mental health before and after the intervention(one dimensions of the 36-item short-form health survey) 8weeks No
Secondary The scores of social functioning before and after the intervention(one dimensions of the 36-item short-form health survey) 8weeks No
Secondary The scores of bodily pain before and after the intervention(one dimensions of the 36-item short-form health survey) 8weeks No
Secondary The scores of general health before and after the intervention(one dimensions of the 36-item short-form health survey) 8weeks No
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