Trial Review

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Trial registered on ANZCTR


Registration number
ACTRN12617000797370
Ethics application status
Approved
Date submitted
23/05/2017
Date registered
31/05/2017
Date last updated
24/04/2020
Date data sharing statement initially provided
24/04/2020
Type of registration
Prospectively registered

Titles & IDs
Public title
The objective Behavioural Assessment of Breaks in SITting and risk of developing gestational diabetes during pregnancy - the BABy-SIT in pregnancy study
Scientific title
Exploring the relationship of post challenge glucose levels and objectively measured sedentary behaviours in mid-term pregnant women
Secondary ID [1] 292020 0
None
Universal Trial Number (UTN)
Trial acronym
The BABy-SIT in pregnancy study
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Pregnancy 303410 0
Gestational diabetes mellitus 303413 0
Condition category
Condition code
Metabolic and Endocrine 302821 302821 0 0
Metabolic disorders
Reproductive Health and Childbirth 302822 302822 0 0
Fetal medicine and complications of pregnancy

Intervention/exposure
Study type
Observational
Patient registry
False
Target follow-up duration
Target follow-up type
Description of intervention(s) / exposure
This is an observational study of sedentary behaviour and sleep patterns in pregnant women attending an outpatient maternity services clinic. Participation involves wearing two small lightweight devices (a sleep monitor and an activity monitor) for a period of 7 days in a 4-week window before the recommended oral glucose tolerance test to screen for gestational diabetes mellitus. The activity monitor (ActivPal) will be worn on the thigh and will provide information on times spent sitting, standing and walking. The sleep monitor (Actigraph) will be worn on the wrist and will provide information on sleeping duration and sleep quality. Participants will choose the timing of the 7-day period within the 4-week window before their oral glucose tolerance test providing that the 7-day period is reflective of their normal weekly schedule.
Intervention code [1] 298151 0
Not applicable
Comparator / control treatment
No control group
Control group
Uncontrolled

Outcomes
Primary outcome [1] 302205 0
Post challenge glucose levels during a pregnancy oral glucose tolerance test
Timepoint [1] 302205 0
Performed at 24-28 weeks gestation
Primary outcome [2] 302207 0
Total accumulated sedentary time, calculated as an average of the total time spent sitting/lying during waking hours (mins/d), as recorded from 7-days of wearing an ActivPal physical activity monitor
Timepoint [2] 302207 0
Measured between 18-28 weeks gestation
Secondary outcome [1] 335169 0
The frequency of interruptions in sitting, defined as the average number of transitions recorded from “sit/lie” posture to “stand” during waking time, as recorded from 7-days of wearing an ActivPAL physical activity monitor
Timepoint [1] 335169 0
Measured between 18-28 weeks gestation.
Secondary outcome [2] 335170 0
Time accumulated in long duration sedentary bouts, defined as the accumulated time spent in bouts >30minutes (mins/d) during waking hours, as recorded from 7-days of wearing the ActivPAL physical activity monitor.
Timepoint [2] 335170 0
Measured between 18-28 weeks gestation
Secondary outcome [3] 335364 0
Total sleep time, defined as the average time spent sleeping (mins/d), as recorded from 7-days of wearing an Actigraph sleep monitor.
Timepoint [3] 335364 0
Measured between 18-28 weeks gestation.
Secondary outcome [4] 335366 0
Sleep efficiency, defined as the time spent sleeping (mins/d) determined from Actigraph sleep monitor divided by time available for sleep ("lights off to lights on"), multiplied by 100 to calculate a percentage.
Timepoint [4] 335366 0
Measured between 18-28 weeks gestation

Eligibility
Key inclusion criteria
This study will recruit pregnant, English-speaking women, aged 18-50 years at 18-27 weeks gestation.
Minimum age
18 Years
Maximum age
50 Years
Sex
Females
Can healthy volunteers participate?
Yes
Key exclusion criteria
Criteria for exclusion include - >28 weeks gestation, multiple pregnancy, known diabetes, taking medications known to affect glucose metabolism, and current smokers.

Study design
Purpose
Natural history
Duration
Cross-sectional
Selection
Convenience sample
Timing
Prospective
Statistical methods / analysis
Using data from the UK Pregnancy Better Eating and Activity Trial (UPBEAT), we estimate that 74 individuals will be required with a minimum power of 80% and a type 2 error probability of 0.05 (two-sided test) to determine whether the association of objectively assessed sedentary time and 2-hour glucose differs from zero. To account for participant attrition and potential for missing devices, we will over-sample by 35% and recruit 100 participants.
Multiple linear regression will be used to assess the association between sedentary time (and its interrelationship with sleep) and glucose outcomes (continuous outcome variable), after adjustment for potential confounders (e.g., age, monitor wear time, pre-pregnancy BMI and pregnancy weight gain).
Binary, multivariate logistic regression models, including confounders (age, monitor wear time, pre-pregnancy weight, pregnancy weight gain) and physical activity time, will be used

Recruitment
Recruitment status
Completed
Date of first participant enrolment
Anticipated
5/06/2017
Actual
26/07/2017
Date of last participant enrolment
Anticipated
1/05/2019
Actual
1/11/2019
Date of last data collection
Anticipated
15/05/2019
Actual
1/11/2019
Sample size
Target
100
Accrual to date
Final
100
Recruitment in Australia
Recruitment state(s)
VIC
Recruitment hospital [1] 8085 0
Mercy Hospital for Women - Heidelberg
Recruitment postcode(s) [1] 16140 0
3084 - Heidelberg

Funding & Sponsors
Funding source category [1] 296551 0
Government body
Name [1] 296551 0
National Health and Medical Research Council (NHMRC)
Country [1] 296551 0
Australia
Primary sponsor type
Individual
Name
Professor David Dunstan
Address
Physical Activity Laboratory
Baker Heart and Diabetes Institute
Level 4, 99 Commercial Rd
Melbourne VIC 3004
Country
Australia
Secondary sponsor category [1] 295506 0
None
Name [1] 295506 0
Address [1] 295506 0
Country [1] 295506 0
Other collaborator category [1] 279582 0
Individual
Name [1] 279582 0
A/Prof Martha Lappas
Address [1] 279582 0
The Mercy Hospital for Women
4th Floor, 163 Studley Rd
Heidelberg VIC 3084
Country [1] 279582 0
Australia

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 297765 0
Mercy Hospital for Women HREC
Ethics committee address [1] 297765 0
Ethics committee country [1] 297765 0
Australia
Date submitted for ethics approval [1] 297765 0
07/02/2017
Approval date [1] 297765 0
18/05/2017
Ethics approval number [1] 297765 0
2017/012

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 75046 0
Prof David Dunstan
Address 75046 0
Physical Activity Laboratory
Baker Heart and Diabetes Institute
Level 4, 99 Commercial Rd
Melbourne VIC 3004
Country 75046 0
Australia
Phone 75046 0
+613 8532 1873
Fax 75046 0
+613 8532 1100
Email 75046 0
[email protected]
Contact person for public queries
Name 75047 0
Robyn Larsen
Address 75047 0
Physical Activity Laboratory
Baker Heart and Diabetes Institute
Level 4, 99 Commercial Rd
Melbourne VIC 3004
Country 75047 0
Australia
Phone 75047 0
+613 8532 1859
Fax 75047 0
+613 8532 1100
Email 75047 0
[email protected]
Contact person for scientific queries
Name 75048 0
Megan Grace
Address 75048 0
Physical Activity Laboratory
Baker Heart and Diabetes Institute
Level 4, 99 Commercial Rd
Melbourne VIC 3004
Country 75048 0
Australia
Phone 75048 0
+613 8532-1855
Fax 75048 0
+613 8532-1100
Email 75048 0
[email protected]

Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
No/undecided IPD sharing reason/comment


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.