Relaxation techniques for postpartum women
Combined Effects Of Progressive Relaxation Techniques Along With Benson Relaxation Techniques on Stress Fatigue and Quality of Life on Postpartum Females
This study is testing if a mix of relaxation techniques can help new moms in Lahore feel less stressed and tired after giving birth.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 54 (estimated) |
| Ages | 20 Years to 40 Years |
| Sex | Female |
| Sponsor | Riphah International University Academic / other |
| Locations | 1 site (Lahore, Punjab Province) |
| Trial ID | NCT06460649 on ClinicalTrials.gov |
What this trial studies
This clinical trial investigates the combined effects of progressive relaxation techniques and Benson relaxation techniques on postpartum women experiencing stress and fatigue. Conducted at Jinnah Hospital in Lahore, participants will be randomly assigned to two groups: one receiving the combined relaxation techniques and the other receiving progressive relaxation with deep breathing exercises. The study aims to assess the impact of these interventions on quality of life and stress levels using validated scales. The trial will last approximately 8 months and will utilize a non-probability convenience sampling method for participant recruitment.
Who should consider this trial
Good fit: Ideal candidates for this study are postpartum women aged 20-40 who are within two weeks of delivery and have no significant postnatal complications.
Not a fit: Patients with severe obesity, psychiatric disorders, or certain medical conditions like diabetes or cancer may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could significantly improve the quality of life and reduce stress for postpartum women.
How similar studies have performed: Other studies have shown positive outcomes using relaxation techniques for stress management in postpartum women, suggesting this approach may be effective.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * • Parity of women must not more than 3 times * Start from 2nd week of postpartum female * Women with aged group of 20- 40 were included in study.(24) * Women who had Vaginal or c section delivery were included in study. * Women with no postnatal complications were included in study Exclusion Criteria: * • Women with Diabetes Militias were excluded * Women with Breast cancer were excluded * Ovarian cancer were excluded * Patient with dementia, delusional disorder were excluded * Women who use Alcohol or substance abuse were excluded * Women who had a history of psychiatric disorders were excluded * Severed obesity ( BMI more than 40)
Where this trial is running
Lahore, Punjab Province
- Jinnah Hospital Lahore — Lahore, Punjab Province, Pakistan (Recruiting)
Study contacts
- Principal investigator: Sabiha Arshad, M.phill — Riphah International University
- Study coordinator: Iqbal Tariq, PhD
- Email: iqbal.tariq@riphah.edu.pk
- Phone: 03458236752
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.