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Combined Effects Of Progressive Relaxation Techniques Along With Benson Relaxation Techniques

R

Riphah International University

Status

Enrolling

Conditions

Postpartum Disorder

Treatments

Other: Benson relaxation techniques
Other: Progressive relaxation techniques

Study type

Interventional

Funder types

Other

Identifiers

NCT06460649
REC/RCR&AHS/23/0586

Details and patient eligibility

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.

Full description

The postpartum (or postnatal) period begins after childbirth and is typically considered to last for six weeks. Postpartum period can be a challenging time for many women, as they often experience increased stress levels, fatigue, and a change in their overall quality of life. 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 when an individual cannot find the right coping skills, which may then become a long term dysfunctional state, hence a chronic psychiatric condition.

The study will be a randomized controlled trial and will be conducted in Jinnah hospital, Lahore. This study will be completed in time duration of 5_6 months after the approval of synopsis. Non probability convenience sampling technique will be used and participants will be recruited in study after randomization. The subjects will be divided into two groups and the 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 5 days 45min per treatment session. After data collection data will be analyzed by using SPSS version 25.

Key words: Fatigue, progressive Relaxation technique, Postpartum period, Postpartum women, Quality of life, Stress

Enrollment

54 estimated patients

Sex

Female

Ages

20 to 40 years old

Volunteers

No Healthy Volunteers

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)

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

54 participants in 2 patient groups

Progressive relaxation techniques+Benson relaxation techniques
Experimental group
Description:
Participants in group A will receive progressive relaxation techniques along benson relaxation sessions will be conducted 3 times a week for 12 weeks . Total number of sessions will be 3
Treatment:
Other: Progressive relaxation techniques
Other: Benson relaxation techniques
Progressive relaxation techniques
Active Comparator group
Description:
Participants in group B will receive progressive relaxation techniques only. Sessions will be conducted 3 times a week for 12 weeks.36 sessions over all
Treatment:
Other: Progressive relaxation techniques

Trial contacts and locations

1

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Central trial contact

Iqbal Tariq, PhD

Data sourced from clinicaltrials.gov

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