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Validation of a Midwifery Model in Palestine 1

Validation of a Midwifery Model in Palestine - Usage and Quality

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03145571
Enrollment
5760
Registered
2017-05-09
Start date
2011-01-01
Completion date
2015-12-31
Last updated
2017-05-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Maternal Health

Brief summary

To validate a model of Continuity of Midwifery Care implemented in the region of Nabuls and Jericho in Palestine in 2013, register data from the Palestinian Ministry of Health will be analyzed for the following indicators related to usage and quality. Changes in these variables before and after the implementation will be compared between the 16 clinics where the model was implemented and all comparable clinics in the region.

Detailed description

In 2013 a program for continuity of midwifery care (midwives at the local hospital provided ante- and post natal care i clinics located in rural villages) in the region Nablus and Jericho on the West Bank, Palestine. By the end of 2013, the model was implemented in 16 of a total of 53 clinics in the region. In order to compare the impact of the continuity of midwifery care on changes in usage of pre- and postnatal services and quality of care, registry data will be obtained from all clinics two years before the implementation (2011-2012) and for two years after the implementation (2014-2015). The following indicators will be compared between the 16 clinics where the program was implemented and comparable clinics where the program has not yet been implemented: 1. Mean number of antenatal visits per woman (Usage primary outcome) 2. Proportion of total pregnant women that visited the clinic (Usage secondary outcome)) 3. Percentage of pregnant referred to higher level of care (Quality primary outcome) 4. Percentage of women referred for high blood sugar levels (Quality secondary outcome) 5. Percentage of women receiving postnatal home visits (Quality primary outcome) 6. Proportion of women seen by doctor after birth (Quality secondary outcome) 7. Proportion of newborns seen by doctor after birth (Quality secondary outcome) 8. Total number of consultations for mother and child after birth (Usage secondary outcome) All data will be obtained from the monthly statistical reports sent from the clinics to the Palestinian Ministry of health. Data sources, statistical procedures, power and sample size: The governmental registry includes data from two years before and two years after the implementation. The registry consists of unidentifiable recordings reported monthly from all clinics to the central statistical database in the Ministry of Health. A copy of the heath authority registry was obtained for statistical analysis. Descriptive and inferential statistics will be used to analyse collected quantitative data. Data will be registered and analysed using the computer statistical package SPSS version 21 and STATA. Prior to analysis all variables will be checked for data file errors.

Interventions

PROCEDUREContinuity of midwifery care

Pre-natal care in rural villages performed by the midwives from the local hospital

Sponsors

Oslo University Hospital
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Intervention model description

Specific output monitored in villages where the program had been implemented, and where it was not implemented

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* All clinics in Nablus and Jericho governorate located in rural areas, that offer pregnancy- and postnatal-care in the whole study period. * Only clinics that had the intervention continuously during the whole observations period (1st of January 2014 and continued till 31st of December 2015) will be included in the intervention group * Only the clinics were there were no intervention at all during the whole period will be included in the control group.

Exclusion criteria

* Clinics located in urban areas (less than three km from Nablus or Jericho city centre). * New Clinics that has not been open during the whole study period. * Clinics were the intervention was only partially implemented

Design outcomes

Primary

MeasureTime frameDescription
Antenatal visits0-9 months before deliveryMean number of antenatal visits in the clinic per woman

Secondary

MeasureTime frameDescription
Referral0-12 months after deliveryPercentage of pregnant referred to higher level of care
Home visits0-12 months after deliveryPercentage of women receiving postnatal home visits

Other

MeasureTime frameDescription
Newborn follow-up0-12 months after deliveryProportion of newborns seen by doctor after birth
Proportion of visits0-9 months before deliveryProportion of total pregnant women that visited the clinic
Consultations post partum0-12 months after deliveryTotal number of consultations for mother and child after birth
Blood sugar referral0-12 months after delivery and 0-9 months before deliveryPercentage of women referred for high blood sugar levels
Doctor follow-up0-12 months after deliveryProportion of women seen by doctor after birth

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 24, 2026