Actively Recruiting
Combined Effects Of Progressive Relaxation Techniques Along With Benson Relaxation Techniques
Led by Riphah International University · Updated on 2024-06-14
54
Participants Needed
1
Research Sites
30 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The postpartum (or postnatal) period begins after childbirth and is typically considered to last for six weeks. Stress is considered a response to any stressor within external or internal milieu, to stay in an adaptive mode using functional or dysfunctional coping skills. It initiates an alterable mode that ultimately becomes a prolonged adaptive struggle The study will be a randomized controlled trial and will be conducted in Jinnah hospital, Lahore. This study will be completed in a time duration of 8 months after the approval of synopsis. Nonprobability convenience sampling technique will be used, and participants will be recruited in study after randomization. The subjects will be divided into two groups and group A will receive progressive relaxation technique along with Benson relaxing technique. and group B will receive progressive relaxation technique and deep breathing exercises will be used as a baseline treatment. The tools that will be used for pre and post treatment assessment are Postpartum fatigue scale (PFS), Perceived Stress Scale (PSS\_10), WHOQOL-BREF Scale. The data will be assessed after 12 weeks. After data collection data will be analyzed by using SPSS version 25.
CONDITIONS
Official Title
Combined Effects Of Progressive Relaxation Techniques Along With Benson Relaxation Techniques
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Women aged 20 to 40 years
- Parity no more than 3 births
- Starting from 2nd week postpartum
- Women who had vaginal or cesarean delivery
- Women with no postnatal complications
You will not qualify if you...
- Women with diabetes mellitus
- Women with breast cancer
- Women with ovarian cancer
- Patients with dementia or delusional disorder
- Women who use alcohol or have substance abuse
- Women with history of psychiatric disorders
- Severe obesity (BMI over 40)
AI-Screening
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Trial Site Locations
Total: 1 location
1
Jinnah Hospital Lahore
Lahore, Punjab Province, Pakistan, 54000
Actively Recruiting
Research Team
I
Iqbal Tariq, PhD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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