Completed

Postpartum Recovery and Coping in Women with Postpartum Hemorrhage

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Study Aim

This study looks at how different coping strategies and interventions affect postpartum recovery and mental health in women who have experienced postpartum hemorrhage.

What is being tested

Interaction Standard Theory-Based Multi-Care Program

+ Conventional Nursing Intervention

Behavioral
Who is being recruted

Urogenital Diseases+7

+ Female Urogenital Diseases and Pregnancy Complications

+ Hemorrhage

From 18 to 39 Years
+15 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Treatment Study

Interventional
Study Start: October 2023
See protocol details

Summary

Principal SponsorXingxing Lv
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: October 1, 2023

Actual date on which the first participant was enrolled.

This study focuses on improving the recovery and overall well-being of women who have experienced postpartum hemorrhage, a serious complication after childbirth. The aim is to explore a new multi-care program that combines different care approaches to better support these women beyond just their physical health. The program includes training for nurses and combines various care techniques, such as psychological support and education about postpartum hemorrhage. The trial involves 110 women admitted to a specific hospital over a year, randomly divided into two groups. One group receives this new, comprehensive care approach, while the other continues with regular nursing care. This research is important as it seeks to address the emotional and psychological needs of these women, which are often overlooked, potentially leading to better recovery and quality of life. Participants in this study are involved in a detailed care program that begins while they are still in the hospital and continues after they are discharged. The program includes personalized care plans, psychological support techniques like empathetic listening and music therapy, and education about their condition. Additionally, there is a focus on diet and physical rehabilitation. To see how well the program works, researchers measure several outcomes, including how the participants cope with stress, their levels of psychological distress, their quality of life, and specific recovery indicators like how quickly they start breastfeeding and how long they stay in the hospital. The study also gathers feedback on how satisfied the women are with the nursing care they receive. This structured approach aims to provide comprehensive support to help women recover not just physically but also mentally and emotionally after experiencing postpartum hemorrhage.

Official TitleThe Effects of an Interaction Standard Theory-Based Multi-Care Program on Postpartum Recovery, Coping Styles, Psychological Distress, and Quality of Life in Women With Postpartum Hemorrhage
NCT07058142
Principal SponsorXingxing Lv
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

110 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Treatment Study

These studies test new ways to treat a disease, condition, or health issue. The goal is to see if a new drug, therapy, or approach works better or has fewer side effects than existing options.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

From 18 to 39 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Urogenital DiseasesFemale Urogenital Diseases and Pregnancy ComplicationsHemorrhagePostpartum HemorrhageObstetric Labor ComplicationsPathologic ProcessesPregnancy ComplicationsPuerperal DisordersPathological Conditions, Signs and SymptomsUterine Hemorrhage

Criteria

7 inclusion criteria required to participate
Delivered in our hospital and received postpartum treatment, with a blood loss >500 mL within 24 hours after delivery;

Age <40 years;

Single live birth at full term;

Stable vital signs;

Show More Criteria

8 exclusion criteria prevent from participating
Cervical laceration (as primary cause of PPH if not manageable by standard protocol and requiring extensive surgical repair beyond typical scope);

Pre-existing severe cardiovascular diseases;

Pre-existing severe renal, cardiac, or hepatic insufficiency;

Known pre-existing coagulation disorders;

Show More Criteria

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

2 intervention groups are designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Experimental
Participants received conventional nursing care plus an interaction standard theory-based multi-care program. This program involved: * Collective training for nursing staff on interaction theories and PPH care. * One-on-one communication to assess patient's psychological state, background, and needs. * Collaborative development of a multi-dimensional care plan. * Specific interventions including: * Hemorrhage Care: Encouraging early breastfeeding, monitoring bleeding, administering uterotonics if needed, abdominal massage. * Psychological Care: Empathetic listening, Satir's communication stances, music therapy, deep breathing, guided imagery. * Cognitive Intervention: Education on PPH causes, treatments, complications using various materials. * Dietary Care: Scientific, balanced dietary plan emphasizing high-calorie, high-protein foods. * Rehabilitation Training: Ensuring warmth, sleep, abdominal massage, gentle vaginal pressure, early ambulation, specific exercises. * Implementation

Group II

Active Comparator
Participants received standard conventional nursing interventions as per the hospital's established protocol for postpartum hemorrhage management. This included careful examination of the soft birth canal and placenta, monitoring vital signs, administering oxygen therapy or blood transfusion if indicated, maintaining communication with the patient's family, and providing basic oral education regarding routine postpartum self-care.

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Suspended

Shijiazhuang Obstetrics and Gynecology Hospital

Shijiazhuang, ChinaOpen Shijiazhuang Obstetrics and Gynecology Hospital in Google Maps
CompletedOne Study Center