UNKNOWNNA

Effect of a Cooperative Education Program Based on Precede-Proceed Model During Pregnancy on Postpartum Depression

This trail aims to evaluate the effects of a cooperative education program based on precede-proceed model during pregnancy on preventing postpartum depression in southern Razavi Khorasan Province.

Sponsor

Gonabad University of Medical Sciences

Enrollment

140 participants

Sites

1 locations

Start Date

November 2019

Completion

November 2019

Post Partum DepressionCooperative Education Program based on Precede-Proceed Model

Enrollment & Timeline

UNKNOWN

Target enrollment (estimated)

Target N

140

participants

Sites

locations

Duration

1 months

total trial span

Rate

140

pts/month needed

Nov 2019Month 82 of 1Nov 2019

100% of trial timeline elapsed

At 1 sites, each site needs to enroll approximately 140.0 patients/month to hit the enrollment target on schedule.

Enrollment target is estimated. ClinicalTrials.gov does not provide real-time enrollment progress.

View on ClinicalTrials.gov

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Primary Outcomes

Postpartum Depression

Edinburgh Postnatal Depression Scale will be filled from baseline to 6 week

Depression in POSTPARTUM WOMEN, usually within four weeks after giving birth (PARTURITION). The degree of depression ranges from mild transient depression to neurotic or psychotic depressive disorders. It includes 10 questions and each question is scored from 0 to 3. The total score ranges from 0 to 30 and a score of 10-13 indicates mild postpartum depression while a score of 14-15 indicates moderate postpartum depression. Score of 16 or higher is considered as severe depression which necessitates introduction to a psychologist.

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Multi-Source Intelligencefrom PubMed · FDA FAERS · WHO ICTRP

No linked publications found in PubMed

PubMed/NCBI (daily updates) FDA FAERS (quarterly updates) WHO ICTRP (weekly updates)

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Fetching protocol from ClinicalTrials.gov…

UNKNOWNNA

Effect of a Cooperative Education Program Based on Precede-Proceed Model During Pregnancy on Postpartum Depression

This trail aims to evaluate the effects of a cooperative education program based on precede-proceed model during pregnancy on preventing postpartum depression in southern Razavi Khorasan Province.

Sponsor

Gonabad University of Medical Sciences

Enrollment

140 participants

Sites

1 locations

Start Date

November 2019

Completion

November 2019

Post Partum DepressionCooperative Education Program based on Precede-Proceed Model

Enrollment & Timeline

UNKNOWN

Target enrollment (estimated)

Target N

140

participants

Sites

locations

Duration

1 months

total trial span

Rate

140

pts/month needed

Nov 2019Month 82 of 1Nov 2019

100% of trial timeline elapsed

At 1 sites, each site needs to enroll approximately 140.0 patients/month to hit the enrollment target on schedule.

Enrollment target is estimated. ClinicalTrials.gov does not provide real-time enrollment progress.

View on ClinicalTrials.gov

Ask AI

Primary Outcomes

Postpartum Depression

Edinburgh Postnatal Depression Scale will be filled from baseline to 6 week

Ask AI

Multi-Source Intelligencefrom PubMed · FDA FAERS · WHO ICTRP

No linked publications found in PubMed

PubMed/NCBI (daily updates) FDA FAERS (quarterly updates) WHO ICTRP (weekly updates)

Ask AI

Eligibility

Sex

female

Healthy Volunteers

Yes

View full criteria

Inclusion Criteria:

* Informed consent to participate in the research
* Gestational age 30-35 weeks
* Be literate
* No history of depression or mental illness in the past
* Healthy fetus on ultrasound

Exclusion Criteria:

* Having a preterm birth
* Refusal to attend training sessions

Ask AI

Effect of a Cooperative Education Program Based on Precede-Proceed Model During Pregnancy on Postpartum Depression

Enrollment & Timeline

Primary Outcomes

Multi-Source Intelligencefrom PubMed · FDA FAERS · WHO ICTRP

Effect of a Cooperative Education Program Based on Precede-Proceed Model During Pregnancy on Postpartum Depression

Enrollment & Timeline

Primary Outcomes

Multi-Source Intelligencefrom PubMed · FDA FAERS · WHO ICTRP

Eligibility

Trial Sites (1)