Clinical Trials Logo

Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04676295
Other study ID # FINNCARE
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date June 1, 2019
Est. completion date December 2024

Study information

Verified date December 2020
Source Helsinki University Central Hospital
Contact Tiina Jääskeläinen, PhD
Phone +358 50 4150274
Email tiina.j.jaaskelainen@helsinki.fi
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

Background: PE (pre-eclampsia) is a common pregnancy-specific vascular hypertensive disease affecting 3-5% of pregnancies. PE independently increases the risk for premature cardiovascular disease (CVD) in mothers and their offspring long-term. PE provides a unique window for early risk profiling and CVD prevention. However, the efficacy of a family oriented lifestyle intervention to lower CVD risk in families with history of PE has not previously been evaluated. Aim: This study will explore the impact of PE on CVD progression 8-12 years from delivery in mothers and their children, and assess whether a lifestyle intervention is useful for lowering mother and child blood pressure and improving the CVD risk profile overall in families with a history of PE. Hypothesis: PE is related with CVD progression mediated by elevated blood pressure. Blood pressure and the CVD risk profile overall is modifiable in mothers and children by a 12-month behavioral lifestyle intervention in families with a history of PE. Study design: Randomized controlled behavioral lifestyle intervention trial where families (mother, child and father from the FINNPEC study) are offered the opportunity to participate in a lifestyle intervention program 8-12 years after a PE pregnancy. 300 PE families will be randomized 1:1 to a 12-month lifestyle intervention program or to a control group. A parallel group of 100 non-PE control families will be assessed at baseline and follow-up. Main outcome: 24 hour mean blood pressure change between baseline and follow-up in mother and child. Significance: This study will provide information on CVD progression in mothers and children 8-12 years from a PE pregnancy. Furthermore, the study assess the effect of a 12-month lifestyle intervention on blood pressure and CVD risk profile overall following a PE pregnancy. Potentially, the study provides the opportunity to identify PE families at highest risk of CVD progression and families amenable to blood pressure and CVD risk profile improvement.


Description:

Power analysis: Power calculations were performed in order to detect 5.5 mmHg reduction in maternal systolic blood pressure with a power of 80% and a 2-sided p-value of 0.05 for the difference between the groups (intervention and control PE) (NICE 2011). Accounting for a 20% loss to follow-up or missing data, a sample of 148 women in the PE intervention group and 148 women in the PE control group is needed. Specific objectives: 1. To assess cardiovascular health and CVD progression in families (mother, child and father) 8-12 years following a PE pregnancy compared with non-PE control families. 2. To assess the effectiveness of a behavioral 12-month lifestyle intervention in mothers and their children 8-12 years following a PE pregnancy to lower blood pressure and improve their CVD risk profile overall. 3. To assess the effectiveness of a lifestyle intervention on the awareness of CVD risk after a PE pregnancy.


Recruitment information / eligibility

Status Recruiting
Enrollment 400
Est. completion date December 2024
Est. primary completion date December 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group N/A and older
Eligibility Inclusion Criteria: Families are recruited from the FINNPEC cohort. In FINNPEC, PE was defined as hypertension and proteinuria occurring after 20 weeks gestation (American College of Obstetricians and Gynecologists 2002 criteria). Hypertension was defined as systolic blood pressure =140 mm Hg or diastolic blood pressure =90 mm Hg. Proteinuria was defined as urinary excretion of =0.3 g protein in a 24-hour specimen, or 0.3 g/L, or two =1+ readings on a dipstick in a random urine determination with no evidence of a urinary tract infection. Each PE diagnosis was ascertained based on hospital records and confirmed independently by a research nurse and a study physician in the original FINNPEC case-control study including 1450 nulliparous or multiparous women with a singleton pregnancy with PE and 1065 pregnant control women without PE (aged 18-47 years) from all 5 university hospitals in Finland during 2008-2011. Exclusion criteria in the FINNPEC: multiple pregnancy, inability to speak Finnish or Swedish. Exclusion Criteria in the FINNCARE: - Pregnancy and/or lactation (for all mothers) - Pre-eclampsia in any previous or subsequent pregnancies (for all non-PE mothers)

Study Design


Intervention

Behavioral:
Face-to-face and web-based lifestyle intervention
Families are provided at baseline with one 60 min face-to-face dietary counseling session with nutritionist using family-oriented motivational interviewing and solution focusing techniques. The intervention continues in an interactive web-based portal where different modules include assignments, activities, and tests and related videos targeting five cardiovascular health-linked behaviors: 1) improving quality of fat in the diet, 2) increasing the consumption of foods rich in fiber, 3) decreasing the use of salt, 4) increasing physical activity and 5) reducing smoking.

Locations

Country Name City State
Finland Helsinki University Hospital Helsinki

Sponsors (2)

Lead Sponsor Collaborator
Helsinki University Central Hospital University of Helsinki

Country where clinical trial is conducted

Finland, 

References & Publications (1)

Jääskeläinen T, Heinonen S, Kajantie E, Kere J, Kivinen K, Pouta A, Laivuori H; FINNPEC Study Group. Cohort profile: the Finnish Genetics of Pre-eclampsia Consortium (FINNPEC). BMJ Open. 2016 Nov 10;6(11):e013148. doi: 10.1136/bmjopen-2016-013148. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Other Arterial wall thickness (mothers) intima-media thickness; common carotid, brachial and radial; mm baseline
Other Left ventricular mass (mothers) left ventricular mass; g baseline
Other Left ventricular systolic function (mothers) left ventricular global longitudinal strain; % baseline
Other Left ventricular diastolic function (mothers) left atrial volume; ml baseline
Other Left ventricular diastolic function (mothers) pulsed wave Doppler mitral early to late inflow velocity ratio (no unit) baseline
Other Left ventricular diastolic function (mothers) mitral lateral annular pulsed wave tissue Doppler early velocity; cm/s baseline
Other Left ventricular diastolic function (mothers) septal pulsed wave tissue Doppler early velocity; cm/s baseline
Other Arterial wall thickness (children) intima-media thickness; common carotid, brachial and radial; mm baseline
Other Left ventricular mass (children) left ventricular mass; g baseline
Other Left ventricular systolic function (children) left ventricular global longitudinal strain; % baseline
Other Left ventricular diastolic function (children) left atrial volume; ml baseline
Other Left ventricular diastolic function (children) pulsed wave Doppler mitral early to late inflow velocity ratio (no unit) baseline
Other Left ventricular diastolic function (children) mitral lateral annular pulsed wave tissue Doppler early velocity; cm/s baseline
Other Left ventricular diastolic function (children) septal pulsed wave tissue Doppler early velocity; cm/s baseline
Primary Blood pressure (mothers) mean 24 hour ambulatory systolic BP and diastolic BP; mmHg baseline -12 months
Primary Blood pressure (children) mean 24 hour ambulatory systolic BP and diastolic BP; mmHg baseline -12 months
Secondary Blood pressure 24 hour variability (mothers) nocturnal systolic and diastolic BP dip; standard deviation of systolic and diastolic BP; weighted standard deviation of systolic and diastolic BP; mmHg baseline -12 months
Secondary Arterial stiffness (mothers) carotid-femoral pulse wave velocity; m/s baseline -12 months
Secondary Adiposity (mothers) BMI; kg/m2 baseline -12 months
Secondary Adiposity (mothers) waist-hip-ratio (no unit) baseline -12 months
Secondary Adiposity (mothers) body fat percentage; % baseline -12 months
Secondary Dietary intake (mothers) food frequency questionnaire on quality of fat (SFA, MUFA and PUFA; E%/day) baseline -12 months
Secondary Dietary intake (mothers) food frequency questionnaire on fiber intake; g/day baseline -12 months
Secondary Dietary intake (mothers) food frequency questionnaire on salt intake; g/d baseline -12 months
Secondary Physical activity and sedentary behavior (mothers) questionnaire data: weekly number of sessions and minutes of moderate-to-vigorous-intensity physical activity and walking baseline -12 months
Secondary Physical activity and sedentary behavior (mothers) questionnaire data: meeting physical activity recommendations baseline -12 months
Secondary Physical activity and sedentary behavior (mothers) questionnaire data: daily minutes of sitting on a non-weekend and weekend day baseline -12 months
Secondary Physical activity and sedentary behavior (mothers) accelerometer data: daily number of steps baseline -12 months
Secondary Physical activity and sedentary behavior (mothers) accelerometer data: daily minutes of total and intensity-specific physical activity baseline -12 months
Secondary Physical activity and sedentary behavior (mothers) accelerometer data: daily minutes of stationary behavior baseline -12 months
Secondary Physical activity and sedentary behavior (mothers) accelerometer data: daily number of breaks in stationary behavior baseline -12 months
Secondary Smoking (mothers) questionnaire on status of smoking/use of snuf/use of electronic cigarettes/nicotine replacement therapy and number of cigarettes/day baseline -12 months
Secondary Laboratory assessment of cardiovascular risk (mothers) lipids (total cholesterol, LDL, HDL, triglycerides; mmol/l) baseline -12 months
Secondary Laboratory assessment of cardiovascular risk (mothers) hs-CRP; mg/l baseline -12 months
Secondary Laboratory assessment of cardiovascular risk (mothers) HOMA index calculated as glucose; mmol/l x insulin; mU/l / 22.5 baseline -12 months
Secondary Awareness of later life morbidity (mothers) A brief questionnaire with true or false questions on pre-eclampsia and later life morbidity baseline -12 months
Secondary Heart rate variability (mothers) standard deviation of all R-R intervals; root mean square of successive R-R interval differences, ms; High frequency power of R-R intervals from spectral band 0.15-0.4 Hz, ms2 ;Low frequency power of R-R intervals from spectral band 0.04-0.15 Hz, ms2 ; and LF/HF ratio baseline -12 months
Secondary Blood pressure 24 hour variability (children) nocturnal systolic and diastolic BP dip; standard deviation of systolic and diastolic BP; weighted standard deviation of systolic and diastolic BP; mmHg baseline -12 months
Secondary Arterial stiffness (children) carotid-femoral pulse wave velocity; m/s baseline -12 months
Secondary Adiposity (children) BMI z-score baseline -12 months
Secondary Adiposity (children) waist-hip-ratio (no unit) baseline -12 months
Secondary Adiposity (children) body fat percentage; % baseline -12 months
Secondary Dietary intake (children) food frequency questionnaire derived data on SFA index, fiber index, salt index (sum of food items rich in SFA/fiber/salt used during the previous week) baseline -12 months
Secondary Physical activity and sedentary behavior (children) questionnaire data: weekly number of days and daily duration of active travel to school and hobbies, structured physical activity outside school hours, unstructured physical activity outside school hours, screen time sitting, non-screen time sitting Accelerometer data: daily number of steps; daily minutes of total and intensity-specific physical activity; daily minutes of and stationary behavior; meeting physical activity recommendations; daily number of breaks in stationary behavior baseline -12 months
Secondary Physical activity and sedentary behavior (children) questionnaire data: weekly number of days and daily duration of active travel to school and hobbies baseline -12 months
Secondary Physical activity and sedentary behavior (children) questionnaire data: structured physical activity outside school hours baseline -12 months
Secondary Physical activity and sedentary behavior (children) questionnaire data: unstructured physical activity outside school hours baseline -12 months
Secondary Physical activity and sedentary behavior (children) questionnaire data: screen time and non-screen time sitting baseline -12 months
Secondary Physical activity and sedentary behavior (children) accelerometer data: daily number of steps baseline -12 months
Secondary Physical activity and sedentary behavior (children) accelerometer data: daily minutes of total and intensity-specific physical activity baseline -12 months
Secondary Physical activity and sedentary behavior (children) accelerometer data: daily minutes of stationary behavior baseline -12 months
Secondary Physical activity and sedentary behavior (children) accelerometer data: meeting physical activity recommendations baseline -12 months
Secondary Physical activity and sedentary behavior (children) accelerometer data: daily number of breaks in stationary behavior baseline -12 months
Secondary Laboratory assessment of cardiovascular risk (children) lipids (total cholesterol, LDL, HDL, triglycerides; mmol/l) baseline -12 months
Secondary Laboratory assessment of cardiovascular risk (children) hs-CRP; mg/l baseline -12 months
Secondary Laboratory assessment of cardiovascular risk (children) HOMA index calculated as glucose; mmol/l x insulin; mU/l / 22.5 baseline -12 months
Secondary Process evaluation: reach participation rate of the families recruited (research database on study visits) baseline
Secondary Process evaluation: reach representativeness of the families participating (parents' and children's age, questionnaire on socio-economics) baseline
Secondary Process evaluation: compliance participation rate in measurements (number of study visits and questionnaires completed) baseline -12 months
Secondary Process evaluation: compliance proportion of sessions completed in the web-based portal (data accumulated in the web-based portal) baseline -12 months
Secondary Process evaluation: acceptability usefulness and ease of use (questionnaire and proportion of webportal sessions completed by the families) baseline -12 months
Secondary Process evaluation: acceptability credibility and satisfaction of the web-based portal (questionnaire and proportion of webportal sessions completed by the families) baseline -12 months
Secondary Process evaluation: acceptability occurrence of technical problems (questionnaire) baseline -12 months
See also
  Status Clinical Trial Phase
Recruiting NCT05650307 - CV Imaging of Metabolic Interventions
Recruiting NCT05654272 - Development of CIRC Technologies
Recruiting NCT04515303 - Digital Intervention Participation in DASH
Completed NCT04056208 - Pistachios Blood Sugar Control, Heart and Gut Health Phase 2
Recruiting NCT04417387 - The Genetics and Vascular Health Check Study (GENVASC) Aims to Help Determine Whether Gathering Genetic Information Can Improve the Prediction of Risk of Coronary Artery Disease (CAD)
Not yet recruiting NCT06211361 - Cardiac Rehabilitation Program in Patients With Cardiovascular Disease N/A
Not yet recruiting NCT06032572 - Evaluation of the Safety and Effectiveness of the VRS100 System in PCI (ESSENCE) N/A
Recruiting NCT04514445 - The BRAVE Study- The Identification of Genetic Variants Associated With Bicuspid Aortic Valve Using a Combination of Case-control and Family-based Approaches.
Enrolling by invitation NCT04253054 - Chinese Multi-provincial Cohort Study-Beijing Project
Completed NCT03273972 - INvestigating the Lowest Threshold of Vascular bENefits From LDL Lowering With a PCSK9 InhibiTor in healthY Volunteers N/A
Completed NCT03680638 - The Effect of Antioxidants on Skin Blood Flow During Local Heating Phase 1
Recruiting NCT04843891 - Evaluation of PET Probe [64]Cu-Macrin in Cardiovascular Disease, Cancer and Sarcoidosis. Phase 1
Completed NCT04083846 - Clinical Study to Investigate the Pharmacokinetic Profiles and Safety of High-dose CKD-385 in Healthy Volunteers(Fed) Phase 1
Completed NCT04083872 - Clinical Study to Investigate the Pharmacokinetic Profiles and Safety of Highdose CKD-385 in Healthy Volunteers(Fasting) Phase 1
Completed NCT03466333 - Postnatal Enalapril to Improve Cardiovascular fUnction Following Preterm Pre-eclampsia Phase 2
Completed NCT03693365 - Fluid Responsiveness Tested by the Effective Pulmonary Blood Flow During a Positive End-expiratory Trial
Completed NCT03619148 - The Incidence of Respiratory Symptoms Associated With the Use of HFNO N/A
Completed NCT04082585 - Total Health Improvement Program Research Project
Completed NCT05132998 - Impact of a Comprehensive Cardiac Rehabilitation Program Framework Among High Cardiovascular Risk Cancer Survivors N/A
Completed NCT05067114 - Solutions for Atrial Fibrillation Edvocacy (SAFE)