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The training effect of coping strategies and relaxation on stress treatment

Comparing the training effects of Coping Strategies and Relaxation on Stress intensity of women who had Uterine Leiomyoma referred to Shiraz Gynecology Clinics-2015

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2016121331387N1
Enrollment
126
Registered
2017-01-13
Start date
2015-09-23
Completion date
Unknown
Last updated
2018-02-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Leiomyoma of uterus. Leiomyoma of uterus, unspecified

Interventions

Intervention 1: In the intervention group 1, will be held 6 sessions of coping strategies, within three weeks (two 90-minute sessions per week). Class content includes: the reception of Position
Problem Definition
brain storming solutions
Decision making
planning to implement the best solution
implementing the selected solution
evaluating the results of the implementation of the solution
what are emotions
need of emotional management skills
Barriers to manage emotions
Cognitive manage of emotions
Negative emotional management strategies ( management of Anger, anxiety and sadness). Intervention 2: In groups 2, will be held beginning a training session relaxation, then will be asked the people
Behavior
In the intervention group 1, will be held 6 sessions of coping strategies, within three weeks (two 90-minute sessions per week). Class content includes: the reception of Position

Sponsors

Vice-Chancellor for Research, Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
20 Years to 45 Years

Inclusion criteria

Inclusion criteria: Inclusion criteria: age 20 to 45 years; evidence of vaginal ultrasound of Uterine Leiomyoma (size 1-7 cm); have mild or moderate stress based on the DASS questionnaires; body mass index below 25; not taking any hormones affecting the size of the leiomyoma from start up to a month after the intervention; not taking any effective drug on stress and depression from start up to a month after the intervention; lack of medical conditions including hypertension, thyroid and diabetes; signing a consent form a conscious; non-participation in any classes or programs affecting stress such as relaxation, yoga and meditation. Exclusion criteria: use of any drug affecting the leiomyoma and stress during the intervention and one month after its completion; the patient's unwillingness to continue to work; absence in more than one session.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Stress. Timepoint: Before the intervention, one and two months after starting intervention. Method of measurement: DASS standard questionnaire.;Leiomyoma size. Timepoint: Before and two months after starting intervention. Method of measurement: Vaginal ultrasound.;The Volume of Menstrual Bleeding. Timepoint: Before and two months after starting intervention. Method of measurement: Number of daily pad.;Pelvic Pain. Timepoint: Before and two months after starting intervention. Method of measurement: VAS.;Urinary Frequency. Timepoint: Before and two months after starting intervention. Method of measurement: Patient reports.;Urgency of Urination. Timepoint: Before and two months after starting intervention. Method of measurement: Patient reports.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactAzam Jokar

Shiraz University of Medical Sciences

jokarhs@yahoo.com+98 71 3647 4255

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026