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Completed

NCT Number: NCT03854331

OBEAT - Beating Obesity

The primary objective of this trial is to study the feasibility of a resilience intervention to reduce stress and thus improve sleep, healthy diet and physical activity in normal weight pregnant women.

Initially, an exploratory study of stressors and worrying in pregnant women will be done by use of qualitative methods (focus group interviews) followed by a randomised controlled feasibility trial with a parallel qualitative process evaluation.

This project is expected to improve the understanding of the processes and feasibility of conducting a randomized intervention study to examine if improvements in chronic stress and poor sleep during pregnancy improves early weight gain and childhood risk of obesity.

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Key information

Age range

18 year–50 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Frederiksberg Hospital

Frederiksberg, 2000, Denmark

About this study

Phase 1: Planning In Phase 1 (6 months), the project will be developed and planned, and approvals from the Danish Data Protection Agency and Ethical Committee of the Capital Region to conduct the study will be obtained.

Validated questionnaires to measure perceived stress, sleep patterns, physical activity- and dietary habits will be selected and pilot tested.

Phase 2: Recruitment and data collection In Phase 2 (12 months), participants will be recruited and randomized. Pregnant women living in Denmark are offered public, antenatal care delivered by hospital employed midwives. Healthy, non-obese, pregnant women assigned to antenatal care and birth at Hvidovre Hospital, are routinely invited to a first antenatal midwife session at gestational week 14-18. At these sessions, participants will be informed and recruited to the feasibility study. In 8 weeks approximately 240 pregnant women will be eligible, thus 120 women corresponding to 50% of all eligible pregnant women in one month will be recruited. In this feasibility study 50% of the women will be randomised to the intervention group and introduced to the resilience internet-based program/ smart phone app and 50% will be randomised to the control group and receive standard care. Computer-based randomization procedures will be used.

Phase 3: Feasibility study evaluation In Phase 3 (19 months), the knowledge obtained in Phase 2 will be evaluated.

An effect evaluation of the project will be conducted by analysing the collected clinical data, primarily related to changes and correlations in chronic stress in mother and infant (measured by hair cortisol), perceived stress, physical activity- and dietary habits, infant birth length and weight, and gestational age.

A process evaluation will also be conducted. The Committee of Health Education will collect data on how much and what parts of the resilience program has been used by the participating pregnant women. In addition, the participants will be asked to complete a short questionnaire on how frequent and how satisfied they have been with using the program. The researchers also want to use qualitative focus group interviews to investigate the participants' attitudes and acceptability of the proposed intervention.

The results of the effect- and process evaluations will be synthesized and will, depending on the results of the feasibility study, be implemented in a following planning of a large RCT.

Qualitative analytical methods The interview guide will be developed based on a literature search of existing literature in the field. To minimize the bias of my own influence I will consider my own experience and pre-understanding as a midwife.

The interviews will be recorded digitally and subsequently transcribed literally. The data will be analyzed using content analysis as described by Graneheim & Lundman. The purpose of the content analysis is to organize and understand the meaning of the data collected in the focus group interviews and to draw conclusions from it.

Statistical analysis The clinical outcomes will be examined using paired t-tests as well as linear or logistic regression analyses. Analyses will be done crude and adjusted for potential confounders obtained from the completed questionnaires. Results of the analyses of the clinical outcomes are expected to be underpowered due to the feasibility design of this study but will however provide estimates indicating any direction or effect size of the resilience program on this target group.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Expecting first child
  • Speaks Danish
  • Non-obese (BMI < 30)
  • Singleton pregnancy
  • Visited to basic level midwife care

Exclusion criteria

  • Non-danish speakers
  • Type 1 or 2 diabetes
  • Visited to specialist midwife care for psychosocial reasons
  • Expecting twins
  • BMI > 30
  • Multipara

Treatment and study plan

Resilience Program

Behavioral

The resilience program consists of different modules that are based on research on mentalization, mindfulness, parent management training, improving self-control and self-efficacy, cognitive behaviour therapy, social learning theory and neuroscience. The MyResilience program is also informed by cognitive bias modification and self-control training research. These techniques have been found to be effective in improving engagement in health behaviours and reducing symptoms and negative behaviours in clinical groups

Primary outcomes

  1. Recruitment-rates - feasibility

    Time frame: Two months after birth

    Number of participants out of eligible pregnant women approached

  2. Recruitment-time - feasibility

    Time frame: Two months after birth

    Number of days used to recruit the decided number of 120 participants

  3. Attrition-rates - feasibility

    Time frame: Two months after birth

    Number of participants leaving the study before the end

  4. Follow up-rates - feasibility

    Time frame: Two months after birth

    Number of participants in final clinical examination

  5. Compliance-rates - feasibility

    Time frame: Two months after birth

    Use of resilience program measured from web-statistics

  6. Self-reported compliance-rates - feasibility

    Time frame: Two months after birth

    Use of resilience program from patient-reported questionnaire

  7. Satisfaction-rates - feasibility

    Time frame: Two months after birth

    Measured from patient-reported questionnaire

Secondary outcomes

  1. Change in maternal chronic stress

    Time frame: Gestational week 14-18, 28, 35, birth and two months after birth

    Assessed by level of cortisol (ng/ml) in 3 cm scalp hair

  2. Change in maternal perceived stress

    Time frame: Gestational week 14-18, 28, 35 and two months after birth

    Assessed by Cohen's Perceived Stress Scale (PSS). PSS measures the respondent's experience of stress over the past four weeks using ten questions to answer to what extent the respondent experiences his life as unpredictable, uncontrollable and stressful, and whether he or she feels nervous or stressed. The scale goes from 0 to 40. The higher the score, the higher the level of stress experienced.

  3. Change in maternal depression, anxiety and tension/stress.

    Time frame: Gestational week 14-18, 28, 35 and two months after birth

    Assessed by The Depression and Anxiety Stress Scale (DASS). DASS is a 42-item self report instrument designed to measure the three related negative emotional states of depression, anxiety and tension/stress. The scale goes from 0 to 42 for every emotional state. The higher the score, the higher the level of depression, anxiety or stress experienced. Range: Stress: Normal 0-10, Mild 11-18, Moderate 19-26, Severe 27-34, Extremely severe 35-42.

    Anxiety: Normal 0-6, Mild 7-9, Moderate 10-14, Severe 15-19, Extremely severe 20-42.

    Depression: Normal 0-9, Mild 10-12, Moderate 13-20, Severe 21-27, Extremely severe 28-42.

  4. Change in mentalization ability

    Time frame: Gestational week 14-18, 28, 35 and two months after birth

    Assessed by the Reflective Functioning Questionnaire, which comprises eight items and includes two subscales: Certainty (RFQc) and uncertainty (RFQu) about mental states. The 7 point Likert scale contains answers ranging from strongly disagree to strongly agree. Of the 6 items on each subscale, two are unique and four shared across the two scales. With the RFQc subscale, strong disagreement reflects hypermentalizing, and agreement to any degree (or a neutral response) reflects more genuine mentalizing (acknowledging the opaqueness of mental states). With the RFQu subscale, high agreement scores reflect a stance characterised by a lack of knowledge about mental states, or 'hypo-mentalizing', and lower scores represent an acknowledgement of the opaqueness of mental states, a characteristic of good mentalizing. Both scales are based on a mean of the 6 items (Cucchi et al. (2018), PeerJ, DOI 10.7717/peerj.5756).

  5. Changes in maternal Sense of Coherence (SOC)

    Time frame: Gestational week 14-18, 28, 35 and two months after birth

    Assessed by Antonovsky's 13-item SOC scale, which measures comprehensibility (5 items), manageability (4 items), and meaningfulness (4 items). Each item has seven graded (Likert-type) response scale, which is summed up and the total scores can range from 13 (low SOC) to the maximum of 91 (highest possible SOC).

  6. Changes in maternal resilience

    Time frame: Gestational week 14-18, 28, 35 and two months after birth

    Assessed by the Connor-Davidson Resilience Scale (CD-risc). The scale comprises of 25 items, each rated on a 5-point scale (0-4). The total score ranges from 0-100, with higher scores reflecting greater resilience.

  7. Differences in parental stress

    Time frame: Two months after birth

    Assessed by The Parental Stress Scale (PSS). PSS is made up of 18 items rated on a Likert- type 5-point scale that describes the parent-child relationship and how each parent feels about it. A higher score indicates a higher level of parental stress.

  8. Changes in fear of childbirth

    Time frame: Gestational week 14-18, 28, 35

    Fear of childbirth is assessed asking the question 'Are you anxious about the course of the upcoming delivery?' in a participant-reported questionnaire. Possible responses are: 'Not at all', 'A little' or 'A lot'. Only the last response is considered to represent fear of childbirth.

  9. Changes in fetal health anxiety

    Time frame: Gestational week 14-18, 28, 35

    Fetal health anxiety is assessed asking the question 'Are you anxious about the health of the expected child?' in a participant-reported questionnaire. Possible responses are: 'Not at all', 'A little' or 'A lot'. Only the last response is considered to represent fetal health anxiety.

  10. Sleep patterns - mother

    Time frame: Gestational week 14-18, 28, 35 and two months after birth

    Self-reported sleep duration and sleep quality measured from participant-reported questionnaire

  11. Changes in participant's physical activity - transportation

    Time frame: Gestational week 14-18, 28, 35 and two months after birth

    Self-reported means of transportation (biking, public transportation, car, walking) in hours pr. week

  12. Changes in participant's physical activity - exercise

    Time frame: Gestational week 14-18, 28, 35 and two months after birth

    Self-reported exercise (i.e. dancing, yoga or badminton) in hours pr. week

  13. Changes in diet - mother

    Time frame: Gestational week 14-18, 28, 35 and two months after birth

    Measured with a Food Frequency Questionnaire (FFQ) developed for the Danish National Birth cohort is used for dietary assessment. Most questions focus on the dietary habits during the 4 weeks prior to completion of the questionnaire, but a number of questions address changes in dietary habits during pregnancy. The FFQ includes questions on intake of 360 food and beverage items in the previous 4 weeks and is validated with a 7-day weighted food record. The 360 food items recorded in the FFQ are aggregated into 36 food groups and, together with the daily intake (in grams) for each food group, eaten by a given individual, are used to identify dietary patterns.

  14. Weight - mother

    Time frame: Gestational week 14-18, 28, 35 and two months after birth

    Maternal weight (kg) measured at midwife sessions

  15. Weight - child

    Time frame: Birth and two months after birth

    Weight (kg), obtained from birth records and clinical examination

  16. Length - child

    Time frame: Birth and two months after birth

    Length (cm) obtained from birth records and clinical examination

  17. Head circumference - child

    Time frame: Birth and two months after birth

    Head circumference (cm) obtained from birth records and clinical examination

Other outcomes

  1. Diet - infant (breastfeeding, bottlefeeding)

    Time frame: Two months after birth

    Measured from participant-reported questionnaire

  2. Infant crying

    Time frame: Two months after birth

    Measured from participant-reported questionnaire in hours of crying pr. day

  3. Differences in infant chronic stress

    Time frame: Birth and two months after birth

    Level of cortisol (ng/ml) in 3 cm scalp hair

  4. Differences in birth method

    Time frame: Birth

    Vaginal birth, elective cesarean og acute cesarean obtained from birth records

  5. Differences in epidural-rate

    Time frame: Birth

    Epidural as pain relief during birth from birth records

  6. Differences in rates of prolonged labour

    Time frame: Birth

    Use of oxytocin-drip during birth from birth records

  7. Differences in use of private healthcare providers

    Time frame: Gestational week 14-18, 28, 35, birth and two months after birth

    Yes/no in participant-reported questionnaire

  8. Differences in absence from work during pregnancy

    Time frame: Gestational week 14-18, 28, 35

    Reasons to absence (i.e. pregnancy complications) and number of days absent in participant-reported questionnaire

Sponsors and collaborators

Lead sponsor

Bispebjerg Hospital

Other

Collaborators

  • Hvidovre University Hospital
  • Oak Foundation
  • TRYG Foundation

Registry information

Official study title

OBEAT - Beating Obesity: A Feasibility Trial

Important dates

Study start
2019
Primary completion
2020
Study completion
2020
First posted
Feb 26, 2019
Registry last updated
Jan 21, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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