NewPreBP: Project Newborn -Preparation for Birth and Parenthood. A Large Interdisciplinary Randomised Trial on the Effect of Birth and Parent Preparation
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 1,766
- 试验地点
- 2
- 主要终点
- Epidural use
研究概览
简要总结
The Danish regions aim to implement antenatal education in small groups for all expectant parents. The effects of general antenatal education for childbirth or parenthood, or both, remain largely unknown. Also it is unknown if antenatal education in small groups is superior to antenatal lectures which is currently standard care.
The aim of the trial is to evaluate if antenatal birth and parent preparation in small groups can increase parenting resources thereby easing birth and creating a smoother and less stressful transition to parenthood among the participants, compared to those allocated to standard care. This in turn is hypothesized to improve health and thriving among newborn families and affect their use of healthcare services. A thorough process evaluation will be conducted highlighting enabling factors and barriers to the implementation. Finally cost-effectiveness analysis will be conducted.
Individually randomised trial sited at Hvidovre Hospital, a large birth clinic in the Copenhagen Capital Region of Denmark.
Participants: 1756 pregnant women ≥ 18 years old, recruited before 20+0 weeks gestation, due to give birth at Hvidovre Hospital. Being legally able and willing to provide signed consent, and being fluent in Danish.
Women are randomised to receive:
- A research-based birth and parenting program. The intervention consists of 4 sessions in small groups that last for 2,5 hours per session at 25, 33 and 35 weeks of gestation, and a post-natal session 5 weeks after expected due date.
- Standard care (control group). The pregnant woman and her partner are offered two antenatal lectures in an auditorium.
The allocation of participants to the intervention will be 1:1 to the intervention and the control group.
Data will be collected via questionnaires at baseline, 37 weeks gestation, 9 weeks post-partum, 6 months post-partum and 1 year post-partum, via the hospital obstetric database, and via the national registers. Analyses will be intention to treat. Subgroup analysis will be conducted in relation to personal and demographic characteristics. Process evaluation will be conducted using questionnaires and qualitative interviews. The incremental societal cost of the intervention will be computed and compared to the measured outcomes in a cost-effectiveness analysis.
Outcomes: Stress, parenting alliance, depressive symptoms, wellbeing obstetric intervention, use of health care services, self-efficacy, divorce.
详细描述
Antenatal education Today Danish antenatal classes are primarily offered in auditoriums as lectures with a minimum of interaction with the audience. The Danish regions currently aim in time to implement antenatal birth and parent preparation classes in small groups for all expectant parents. However, it is unknown if 1) antenatal preparation in small groups is superior to standard care; 2) what elements the preparation should encompass to meet the needs of expectant parents today; and 3) what the cost-effectiveness of antenatal preparation in small groups is compared to large-scale preparation in auditoriums.
Trial objectives and purpose The primary aim is to compare parenting resources, health and thriving, and use of healthcare services in newborn families enrolled in a research-based standardised antenatal birth and parenting program in small groups with those allocated to standard care.
Development of the program: We have developed a comprehensive, theoretically founded parenting program in collaboration with midwives, health care visitors, a psychologist and family therapist, parents, and leading national and international researchers and clinicians in this field.
Process evaluation: Focus group interviews with service providers, group facilitators and participants will be carried out. Program fidelity e.g. whether the protocol is followed in program delivery, and how much of the intended program the participants are receiving, as well as program reach e.g. what proportions of the intended groups are participating in the program, has an impact on the effect of an intervention. We will evaluate whether the protocol is followed in program delivery and how much of the intended program the participants are receiving. Participants will be asked to fill in an electronic questionnaire on-site at the end of each session. The questionnaire will highlight whether the intended subjects of the session have been covered as well as to what extent the participants found the information given useful. Group facilitators will be asked to fill in a similar questionnaire with the opportunity to explain why certain topics may have been omitted.
Non respondent/non-participation: What proportions of the intended groups are participating in the program will be explored by examining demographic characteristics of those who declined to participate in the trial via the national registers, as well as examining characteristics of those who accepted and then did or did not show up for the sessions.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Prevention
- 盲法
- Single (Outcomes Assessor)
入排标准
- 年龄范围
- 18 Years 至 —(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Expectant pregnant women (and partners)
- •≥ 18 years old
- •Due to give birth at Hvidovre Hospital, Denmark
- •Able to speak and understand Danish
- •Being legally able and willing to provide signed consent
排除标准
- •Not providing signed informed consent
结局指标
主要结局
Epidural use
时间窗: during labour
Epidural use during will be measured using data from the hospital obstetric database
次要结局
- Perceived stress(baseline, 37 weeks gestation, 9 weeks post-partum, 6 months post-partum, 1 year post-partum)
- Parenting alliance(6 months post-partum, 1 year post-partum)
- Parenting stress(9 weeks post-partum, 6 months post-partum, 1 year post-partum)
研究者
Vibeke Koushede
Principal Investigator
University of Southern Denmark
