- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06304311
Effectiveness of Backside Massage and Lamaze Breathing on Labour Outcome Among Primigravida
Effectiveness of Backside Massage and Lamaze Breathing on Labour Outcome Among Primigravida in Tertiary Care Hospitals, Lahore Pakistan: A Randomized Control Trial
Study Overview
Status
Conditions
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Punjab Province
-
Lahore, Punjab Province, Pakistan, 54000
- Lady Wallingdon Hospital
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Description
Inclusion Criteria:
- Primigravidae
- Age 20-35 years old
- Gestational age of 37-41 weeks
- First stage of labour
- Singleton pregnancy
- Cephalic presentation
- Regular contractions
- Cervical dilatation of at least 6 cm
- Minimum of three contractions every 10 minutes
- Contraction intensity of at least moderate
- Contraction duration between 30 seconds and 60 seconds
Exclusion Criteria:
- Diagnosis of underlying chronic diseases (e.g., cardiovascular disease, kidney disease, diabetes, asthma, mental health disorders, epilepsy or seizure)
- Pregnancy-related diseases (e.g., gestational diabetes, preeclampsia, cephalo-pelvic disproportion, polyhydramnios or oligohydramnios, deep venous thrombosis)
- Pregnancy complications (e.g., placenta praevia, antepartum haemorrhage, fetal distress, administration of analgesics)
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Supportive Care
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Active Comparator: Routine Obstetrics care (Control)
Participants in the control arm received routine obstetrics care, which typically includes standard prenatal care, monitoring during labor, and delivery management according to established hospital protocols.
There were no additional interventions or techniques implemented beyond standard practice for managing labor and delivery.
|
Participants in the control arm received routine obstetrics care, which typically includes standard prenatal care, monitoring during labor, and delivery management according to established hospital protocols.
There were no additional interventions or techniques implemented beyond standard practice for managing labor and delivery.
|
|
Experimental: Routine Obstetrics care & Lamaze breathing techniques and backside massage (Interventional group)
Participants in the experimental arm received routine obstetrics care, similar to the control group, along with additional interventions of Lamaze breathing techniques and backside massage.
Lamaze breathing techniques were taught to participants during antenatal classes or individual sessions, focusing on deep breathing, relaxation, and pain management strategies during labor.
Backside massage was administered by trained personnel using gentle, rhythmic strokes on the lower back to alleviate discomfort and promote relaxation during labor.
These interventions were integrated into the labor and delivery process alongside routine obstetrics care.
|
Lamaze breathing techniques Five breathing patterns were introduced namely- cleansing breathing for relaxation, slow-paced breathing, modified-paced breathing and patterned- paced breathing. These patterns were used during and following contractions. Gentle pushing, and breath-hold during pushing were instructed during the second stage of labor which encouraged descent of the baby. Backside massage during 2nd stage of labor by the trained massage therapist. |
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Labour pain intensity
Time Frame: During 1st stage to 01 day after labour
|
Labour pain intensity is a measure used to assess the severity or level of pain experienced by a woman during childbirth.
It typically involves asking the woman to rate her pain on a scale, often ranging from 0 to 10, with 0 representing no pain and 10 representing the worst pain imaginable.
This outcome measure helps healthcare providers understand the woman's level of discomfort during Labour and can guide decisions regarding pain management strategies and interventions to ensure her comfort and well-being throughout the birthing process.
|
During 1st stage to 01 day after labour
|
|
Anxiety level
Time Frame: During 1st stage to 01 day after labour
|
Anxiety levels were measured by GAD-7 scoring system.
GAD-7 is a brief self-report questionnaire designed to screen for generalized anxiety disorder and assess its severity.
It consists of 7 items, and participants rate how often they have been bothered by each symptom over the past two weeks on a scale from 0 to 3. Total scores range from 0 to 21, with higher scores indicating more severe anxiety symptoms.
|
During 1st stage to 01 day after labour
|
|
Duration of Labour
Time Frame: During 1st stage to 01 day after labour
|
Duration of labour is a measure used to assess the length of time it takes for a woman to progress through the stages of childbirth, from the onset of regular contractions to the delivery of the baby and placenta.
It is typically recorded in hours or minutes and includes the duration of both the active and passive phases of labour, as well as the length of time spent pushing during the second stage.
Monitoring the duration of labour is essential for healthcare providers to evaluate the progress of labour, identify potential complications, and make informed decisions regarding interventions or assistance to ensure a safe and healthy delivery for both the mother and baby.
|
During 1st stage to 01 day after labour
|
|
Maternal self-efficacy
Time Frame: During 1st stage to 01 day after labour
|
Childbirth Self-Efficacy Inventory (CBSEI) for the measurement of maternal confidence & self-efficacy By Nancy.
K. Lowe, for the experimental and control group.
(Tool indicates 1 which indicates not all helpful and 10 very helpful)
|
During 1st stage to 01 day after labour
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Study Chair: Prof. Dr. Lim Gek Mul, Masha University
- Study Director: Prof. Dr. Rusli Bin Nordin, Masha University
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- MAHSA/PHD/SON/2024/01
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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