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Trial registered on ANZCTR
Registration number
ACTRN12611000331932
Ethics application status
Approved
Date submitted
28/03/2011
Date registered
29/03/2011
Date last updated
29/03/2011
Type of registration
Prospectively registered
Titles & IDs
Public title
Health In Pregnancy and Post Birth: The HIPP Study
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Scientific title
A Randomised Controlled Trial of a Specialised Health Coaching Intervention to Prevent Excessive Gestational Weight Gain and Postpartum Weight Retention
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Secondary ID [1]
253200
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Nil
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Universal Trial Number (UTN)
Nil
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Trial acronym
HIPPS
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Obesity
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Gestational weight gain
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Condition category
Condition code
Diet and Nutrition
258882
258882
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0
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Obesity
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Reproductive Health and Childbirth
258883
258883
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0
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Childbirth and postnatal care
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Mental Health
258885
258885
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0
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Studies of normal psychology, cognitive function and behaviour
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
Health Coaching, Education Alone
Health Coaching: In addition to the usual care, women in this condition will take part in a Health Coaching intervention program. Our specialised Health Coaching intervention has two components: (1) one-on-one sessions with a Health Coach, and (2) educational group sessions lead by a Health Coach, with key topics the same as described below for the Education Alone group education sessions but with Health Coaching included as well. The two components will be run concurrently for the Intervention group.
- Initial meeting with Health Coach at 14-16 weeks gestation
- First Health Coaching session at 16-18 weeks gestation (face-to-face, 1 hour duration)
- First group education session (Intervention group only) at 20 weeks gestation
- Second group education session (Intervention group only) at 22 weeks gestation
- Second session with Health Coach at 24 weeks gestation (telephonic, 30 mins duration)
- Two brief follow-up sessions with Health Coach between 28-30 weeks (telephonic, 15 mins duration each)
Education Alone: Women in this condition will only receive two education group sessions run by an educator (not a Health Coach) that include the following key topics: dietary and physical activity guidelines in pregnancy; beliefs about pregnancy weight gain and body image; beliefs about postpartum weight loss and body image; mood changes during pregnancy; factors that protect a women against elevated depressive symptoms; and the negative consequence of postpartum weight retention for maternal and infant/child health.
- First group education session (Education Alone group only) at 20 weeks gestation
- Second group education session (Education Alone group only) at 22 weeks gestation
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Intervention code [1]
257678
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Prevention
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Intervention code [2]
264130
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Lifestyle
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Intervention code [3]
264131
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Behaviour
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Comparator / control treatment
Usual care: Women in this condition will be case-managed by their obstetrician, midwife or GP as would normally happen. This is the pathway available to the majority of pregnant women in the state of Victoria. Women will be assessed at baseline for current and pre-pregnancy BMI by the research fellow appointed to the study and will have follow-up assessments at the same time as the intervention women.
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Control group
Active
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Outcomes
Primary outcome [1]
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Body Mass Index (BMI)
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Assessment method [1]
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Timepoint [1]
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16-18 weeks gestation, 32 weeks gestation, at birth, 6 weeks postpartum, 6 months postpartum, 12 months postpartum
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Secondary outcome [1]
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Readiness to Change (Readiness to Change 12-item measure, questionnaire)
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Assessment method [1]
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Timepoint [1]
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16-18 weeks gestation, 32 weeks gestation, 6 weeks post partum, 6 months postpartum, 12 months postpartum
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Secondary outcome [2]
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Motivation to change (12-item Change measure, questionnaire)
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Assessment method [2]
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Timepoint [2]
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16-18 weeks gestation, 32 weeks gestation, 6 weeks post partum, 6 months postpartum, 12 months postpartum
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Secondary outcome [3]
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General distress & psychopathology (Rosenberg Self Esteem Scale, State-Trait Anxiety Inventory, Beck Depression Inventory, Edinburgh Postnatal Depression Scale)
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Assessment method [3]
266481
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Timepoint [3]
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16-18 weeks gestation, 32 weeks gestation, 6 weeks post partum, 6 months postpartum, 12 months postpartum
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Secondary outcome [4]
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Body dissatisfaction (Body Attitudes Questionnaire, Pregnancy Figure Rating Scales, Contour Drawing Rating Scales)
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Assessment method [4]
266482
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Timepoint [4]
266482
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16-18 weeks gestation, 32 weeks gestation, 6 weeks post partum, 6 months postpartum, 12 months postpartum
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Secondary outcome [5]
266483
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Physical activity (Active Australia Survey)
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Assessment method [5]
266483
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Timepoint [5]
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16-18 weeks gestation, 32 weeks gestation, 6 weeks post partum, 6 months postpartum, 12 months postpartum
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Secondary outcome [6]
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Food intake (National Nutrition Survey Food Frequency Questionnaire)
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Assessment method [6]
266484
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Timepoint [6]
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16-18 weeks gestation, 32 weeks gestation, 6 weeks post partum, 6 months postpartum, 12 months postpartum
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Eligibility
Key inclusion criteria
Pregnant women who have a BMI >18.5 (American IOM cut-off for normal weight), are 18 years of age or older, English speaking, less than 18 weeks gestation
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Minimum age
18
Years
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Maximum age
No limit
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Sex
Females
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Can healthy volunteers participate?
Yes
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Key exclusion criteria
History of disordered eating or diabetes, non-English speaking, greater than 18 weeks gestation
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Study design
Purpose of the study
Prevention
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Allocation to intervention
Randomised controlled trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
A total of 264 women will be recruited; 132 women randomly assigned into the Health Coaching intervention, 132 women into the education alone group; an additional 132 women have been recruited in another active usual care control group which will be used as a comparison. Concealment of allocation of women to each group will be performed via central randomisation by computer.
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
A permuted blocks randomised treatment allocation schedule, produced by computer algorithm, will be used for this randomisation process.
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Masking / blinding
Blinded (masking used)
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Who is / are masked / blinded?
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Intervention assignment
Parallel
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Other design features
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Phase
Not Applicable
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Type of endpoint/s
Efficacy
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Statistical methods / analysis
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Recruitment
Recruitment status
Not yet recruiting
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Date of first participant enrolment
Anticipated
1/05/2011
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Actual
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Date of last participant enrolment
Anticipated
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Actual
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Date of last data collection
Anticipated
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Actual
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Sample size
Target
220
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
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Recruitment postcode(s) [1]
3484
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Eastern metropolitan Melbourne
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Funding & Sponsors
Funding source category [1]
258152
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Government body
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Name [1]
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National Health and Medical Research Council (NHMRC)
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Address [1]
258152
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National Health and Medical Research Council
GPO Box 1421
Canberra ACT 2601
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Country [1]
258152
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Australia
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Primary sponsor type
University
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Name
Deakin University
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Address
Deakin University
Burwood Highway, Burwood, Victoria 3125
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Country
Australia
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Secondary sponsor category [1]
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Individual
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Name [1]
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Associate Professor Helen Skouteris
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Address [1]
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School of Psychology
Deakin University
221 Burwood Highway, Burwood, Victoria 3125
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Country [1]
257316
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Australia
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Secondary sponsor category [2]
263808
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Individual
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Name [2]
263808
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Professor Marita McCabe
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Address [2]
263808
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School of Psychology
Deakin University
221 Burwood Highway, Burwood, Victoria 3125
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Country [2]
263808
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Australia
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Other collaborator category [1]
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Individual
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Name [1]
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Professor Jeannette Milgrom
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Address [1]
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Department of Psychology
School of Behavioural Science
University of Melbourne
Melbourne VIC 3081
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Country [1]
251691
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Australia
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Other collaborator category [2]
251692
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Individual
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Name [2]
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Professor Bridie Kent
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Address [2]
251692
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School of Nursing and Midwifery
Deakin University
221 Burwood Highway
Burwood VIC 3125
Australia
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Country [2]
251692
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Australia
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
260132
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Eastern Health HREC
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Ethics committee address [1]
260132
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Eastern Health Research and Ethics Committee 5 Arnold Street Box Hill, Victoria 3128 PO Box 94, Box Hill, Victoria 3128 ethics@easternhealth.org.au
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Ethics committee country [1]
260132
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Australia
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Date submitted for ethics approval [1]
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25/01/2011
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Approval date [1]
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25/03/2011
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Ethics approval number [1]
260132
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E40/1011
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Summary
Brief summary
The aim of this project is test the effects of an intervention we have designed that targets behavioural changes in relation to eating and physical activity as well as changes in psychological factors such as motivation, confidence, mood, and body image concerns, with the aim of maintaining healthy weight gain during pregnancy.
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Trial website
TBA
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Trial related presentations / publications
Skouteris, H., Hartley-Clark, L., McCabe, M., Milgrom, J., Kent, B., Herring, S., & Gale, J. (2010). Preventing excessive gestational weight gain: A systematic review of interventions. Obesity Reviews, 11, 757 – 768. ERA Ranking A*
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Public notes
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Contacts
Principal investigator
Name
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Address
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Country
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Phone
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Fax
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Email
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Contact person for public queries
Name
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Associate Professor Helen Skouteris
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Address
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School of Psychology
Deakin University
221 Burwood Highway
Burwood Victoria 3125
Australia
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Country
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Australia
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Phone
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61 3 9251 7699
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Fax
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61 3 9244 6858
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Email
15211
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[email protected]
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Contact person for scientific queries
Name
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Associate Professor Helen Skouteris
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Address
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School of Psychology
Deakin University
221 Burwood Highway
Burwood Victoria 3125
Australia
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Country
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Australia
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Phone
6139
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61 3 9251 7699
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Fax
6139
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61 3 9244 6858
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Email
6139
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[email protected]
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No information has been provided regarding IPD availability
What supporting documents are/will be available?
No Supporting Document Provided
Results publications and other study-related documents
Documents added manually
No documents have been uploaded by study researchers.
Documents added automatically
No additional documents have been identified.
Download to PDF