NCT07077577

Brief Summary

This quasi experimental qualitative study aims to investigate whether Holistic Birth Approaches is useful technique for improved women's child birth experience. The study objectives include investigating the effect of holistic birth strategies on birth process and how it addresses the fear and anxiety issues during child birth. Moreover, measuring level of satisfaction among women who received holistic strategies during birth was also included in this study. Investigator will also examine the importance of holistic approach for labor pain and delivery management. The study will be conducted in chosen public healthcare facilities that either offers or gives holistic birth methods. The women in labor pain who arrived at hospital where holistic approach is offered for delivery will be included for study.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
14

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Apr 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

April 5, 2025

Completed
Same day until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 5, 2025

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

June 5, 2025

Completed
13 days until next milestone

First Submitted

Initial submission to the registry

June 18, 2025

Completed
1 month until next milestone

First Posted

Study publicly available on registry

July 22, 2025

Completed
Last Updated

July 22, 2025

Status Verified

July 1, 2025

Enrollment Period

Same day

First QC Date

June 18, 2025

Last Update Submit

July 20, 2025

Conditions

Outcome Measures

Primary Outcomes (1)

  • Benefits of Holistic Birth Approach Use

    Pre Intervention; Evaluating pregnant women perspectives, experiences, knowledge and expectations before receiving any holistic birth approach Intervention Phase: Holistic Birth Approaches employed to women Post Intervention; Birth Experiences after receiving Holistic Birth Approach use

    Pre Intervention interviews: Pre-delivery (when women got admitted to hospital for delivery) Intervention: At time of delivery Post Intervention interviews: Post-delivery (within one or two days after delivery when women was comfortable for interviews)

Study Arms (1)

Use of Holistic Approach techniques during delivery, single arm quasi experimental study

EXPERIMENTAL

this is single arm quasi experimental study in which intervention is given to women at time of delivery

Procedure: Holistic Birth Approach

Interventions

Holistic Birth Approach involves use of non pharmacological techniques for better labor process management with less experience of pain, fear and maternal satisfaction to women delivering the baby through normal delivery method.

Use of Holistic Approach techniques during delivery, single arm quasi experimental study

Eligibility Criteria

Age18 Years - 40 Years
Sexfemale(Gender-based eligibility)
Gender Eligibility Detailsfemale
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Pregnant reproductive age women (18-40 years) who will be willing to participate and understand Urdu language will be include in study who arrived at public health care facility for delivery and is experiencing labor pain The women from those healthcare facilities will be include that provides holistic birth approaches to women for improved birth experience particularly for labor pain, fear of birth and mother's satisfaction

You may not qualify if:

  • Those who are not willing for interview will not be included in study. Women having serious medical condition requiring inpatient and outpatient care. Women younger than 18 and more than 40 years.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

hospital from Southern Punjab

Dera Ghazi Khan, Punjab Province, 32200, Pakistan

Location

MeSH Terms

Conditions

Labor Pain

Condition Hierarchy (Ancestors)

PainNeurologic ManifestationsSigns and SymptomsPathological Conditions, Signs and Symptoms

Study Officials

  • Dr Nadia Maryam, Mphil PH

    University of the Punjab

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
SUPPORTIVE CARE
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor of Public Health

Study Record Dates

First Submitted

June 18, 2025

First Posted

July 22, 2025

Study Start

April 5, 2025

Primary Completion

April 5, 2025

Study Completion

June 5, 2025

Last Updated

July 22, 2025

Record last verified: 2025-07

Data Sharing

IPD Sharing
Will not share

due to the issues of confidentiality and privacy of patients data will not be shared

Locations