Trial Review

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Trial registered on ANZCTR


Registration number
ACTRN12611000064909
Ethics application status
Approved
Date submitted
17/12/2010
Date registered
18/01/2011
Date last updated
23/09/2024
Date data sharing statement initially provided
23/09/2024
Date results provided
23/09/2024
Type of registration
Retrospectively registered

Titles & IDs
Public title
The ’40-Something’ Study: Preventing weight gain prior to menopause
Scientific title
The ’40-Something’ Study: A pilot weight control randomised controlled trial for healthy weight and overweight mid-age pre-menopausal women.
Secondary ID [1] 253305 0
Nil
Universal Trial Number (UTN)
U1111-1118-1612
Trial acronym
nil
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Weight gain 258838 0
Abdominal Obesity 260973 0
Condition category
Condition code
Diet and Nutrition 258977 258977 0 0
Obesity

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
Equal numbers of healthy weight (BMI of 18.5-24.9kg/m2) and overweight (BMI 25-29.9kg/m2 ) women (44-50 years and still pre-menopausal) will be recruited and randomly allocated to an Intensive Intervention group (4 individual sessions with a Dietitian and 1 with an Exercise Physiologist) or to an Information Only control group over a 12 month period.
1. Intensive Intervention participants:
Each intensive intervention participant will each have five consultations with a health professional (4 with a Dietitian and 1 with an Exercise Physiologist) who will be registered Medicare providers. The professionals will be trained to promote changes in dietary intake and physical activity (PA) in order to achieve weight control goals using a written protocol, developed by researchers using Clinical Best Practice Weight Management Guidelines and principles of motivational interviewing (see point 2 for detail). The women will be provided with print materials as detailed below.
Appointment 1-(baseline) 60 minutes with Dietitian: Discuss current weight and set weight maintenance/loss goals. Assess motivation levels. Provide dietary advice to consume a high nutritional quality diet providing around 8300kJ/6300kJ per day. Use a social cognitive framework to identify environmental barriers and find strategies to overcome them by increasing self efficacy. Provide pamphlet: ‘Weight control: how to maintain your weight as you approach menopause’ to healthy weight women or ‘Weight control: how to lose weight as you approach menopause’ to those overweight at baseline.
Appointment 2- (baseline) 60 minutes with Exercise Physiologist: Discuss current PA levels and exercise experience. Conduct pre-exercise screening, assess injury history and determine exercise self efficacy. Evaluate compliance with current guidelines (150 mins/wk for healthy weight and 250mins/wk for overweight women as well as less than 3 hours/day sitting time) and discuss barriers and facilitators. Set goals for lifestyle PA (monitored by pedometers) and provide individualised exercise training program consisting of progressive resistance training and aerobic activity.
Appointment 3 (3 months) 45 minute appointment with Dietitian: Check weight and discuss any weight change. Provide weight maintenance advice for overweight women reaching goal weight. Assess motivation. Discuss compliance with dietary advice using 4 day food record and pedometer data and discuss any barriers arising.
Appointment 4 (6 months) 45 minute appointment with Dietitian: Check weight and discuss any weight change. Assess motivation. Discuss any barriers arising.
Appointment 5 with Dietitian (9 months) 45 minute appointment with Dietitian: As per appointments 3 and 4 months, plus provide further weight maintenance advice. Advise how to stay motivated. Provide contact details for any queries.
2. Motivational interviewing (MI)
Motivational interviewing techniques will be used by the practitioners DURING the interviews. this is not additional to the procedures described- it is the PROCESS that will be used. MI is used as an approach where the weight change goals and behaviour changes for dietary intake and physical activity are suggested by the client to promote autonomy. The dietitian and exercise physiologist faciltate this process. Participants are encouraged to take responsibility for their own changes. The communication style on the part of the participants is non-directive; it is questioning, reflective and affirming. The interviews will be audio-recorded, and evaluated by an experienced psychologist for compliance with MI techniques.
Intervention code [1] 257754 0
Prevention
Intervention code [2] 257755 0
Lifestyle
Intervention code [3] 257756 0
Behaviour
Comparator / control treatment
Information Only control group
The control group women will receive written materials to prevent attrition from demoralisation. The materials will be identical to those provided to the intervention women. the only difference is that the control group women will receive the materials by mail while the intervention group women received them face to face.
Women who are healthy weight at baseline will receive materials on how to achieve an energy intake of 8300kJ/day and 150 min/week physical activity in the pamphlet: ‘Weight control: how to maintain your weight as you approach menopause’

Women who are overweight at baseline will receive materials detailing how to achieve an energy intake of 6300kJ/day and 250min/week of physical activity in the pamphlet: ‘Weight control: how to lose weight as you approach menopause’.
Control group
Active

Outcomes
Primary outcome [1] 259830 0
1. Body weight (kg) measured in light clothing, without shoes on a digital scale to the nearest 0.01 decimal, using Omron HBR-500 Body Composition Scales (Omron Healthcare Co. Ltd. Japan).
Timepoint [1] 259830 0
Baseline, 3 months and 12 months after commencing intervention to assess intervention effects, then 18 and 24 months after intervention commencement to assess maintenance.
Primary outcome [2] 259831 0
2. Waist Circumference (cm) - Waist circumference measured at the narrowest point. Each measurement will be recorded with a non-extensible steel tape (KDSF10-02, KDS Corporation, Osaka, Japan).
Timepoint [2] 259831 0
Baseline, 3 months and 12 months after commencing intervention to assess intervention effects, then at 24 months after intervention commencement to assess maintenance.
Secondary outcome [1] 268667 0
1. Body Mass Index (BMI) - Height will be measured to 0.1 cm using the stretch stature method and a stadiometer (Veeder-Root (VR) High Speed Counter) (Harpenden/Holtain, Mentone Education Centre, Morrabin, Victoria). BMI will be calculated using the standard equation (weight [kg]/height[m]2).
Timepoint [1] 268667 0
Baseline, 3 months and 12 months after commencing intervention to assess intervention effects, then at 18 and 24 months after intervention commencement to assess maintenance.
Secondary outcome [2] 268668 0
2. Systolic and diastolic blood pressure and resting heart rate will be measured using a NISSEI/DS-105E digital electronic blood pressure monitor (Nihon Seimitsu Sokki Co. Ltd., Gunma, Japan) under standardized procedures
Timepoint [2] 268668 0
Baseline, 3 months and 12 months after commencing intervention to assess intervention effects, then at 24 months after intervention commencement to assess maintenance.
Secondary outcome [3] 268669 0
3. Physical activity measured using Yamax SW700 pedometers (Yamax Corporation, Kumamoto City, Japan). Participants will be asked to wear pedometers for four consecutive days and keep to their normal routine. At baseline assessments, participants will be instructed on how to attach the pedometers (at the waist on the right hand side) and asked to remove the pedometers only when sleeping, when the pedometer might get wet (e.g. swimming, showering) or during contact sports. At the end of the day participants were instructed to record their steps and reset their pedometers to zero. Once they had completed four days of monitoring, participants will be instructed to return it to the research team.
Timepoint [3] 268669 0
Participants will wear pedometers for 4 days at baseline and then again at 3 and 12 months after beginning the intervention.
Secondary outcome [4] 268670 0
4. 4 day Weighed Food Record (WFR)
Dietary intake will be measured through a 4 day WFR. Participants will be trained how to accurately complete the diary according to a developed protocol. The women will be instructed to complete the WFR over 4 consecutive days, including one weekend day (Wednesday to Saturday or Sunday to Wednesday). Participants will be provided with electronic kitchen scales sensitive to 0.1 decimal points (Salter Electronic Kitchen Scale; Salter Housewares Tonbridge England) to record the weight, in grams, of all food, beverages and leftovers at the time of consumption. They will be given the booklet ?Your diet and physical activity diary? for the purpose of recording the information. Detailed descriptions of foods are requested, including the brands of packaged foods, alcohol, water, snacks and cooking methods. Participants are encouraged not to change usual eating habits whilst completing the diary.
Timepoint [4] 268670 0
Measured at baseline, 3 months and 12 months after beginning the intervention
Secondary outcome [5] 268671 0
5. Food portion sizes will be assessed using items from the Cancer Council Victoria (CCV) Dietary Questionnaire for Epidemiological Studies (DQES v2)
Timepoint [5] 268671 0
Measured at baseline and 12 months after beginning the intervention
Secondary outcome [6] 268672 0
6. Physical activity and dietary restraint using validated questionnaires
Timepoint [6] 268672 0
Baseline, 3 months and 12 months after commencing intervention to assess intervention effects, then at 24 months after intervention commencement to assess maintenance.
Secondary outcome [7] 268673 0
7. Perceived physical and mental health using the Short Form 36 (SF-36) questionnaire
Timepoint [7] 268673 0
Baseline and 12 months after commencing intervention to assess intervention effects, then at 24 months after intervention commencement to assess maintenance.
Secondary outcome [8] 268674 0
8. Percentage Fat, Skeletal Muscle mass and resting metabolic rate using BIA Omron HBR-500 Body Composition Scales (Omron Healthcare Co. Ltd. Japan). scales
Timepoint [8] 268674 0
Baseline, 3 months and 12 months after commencing intervention to assess intervention effects, then at 18 and 24 months after intervention commencement to assess maintenance.
Secondary outcome [9] 268675 0
9. Sedentary behaviours: will be assessed by a validated questionnaire from Brown et al. Medicine and Science in Sports and Exercise (MSSE) (in press)Timepoint: Measured at baseline and 12 months after beginning the intervention
Timepoint [9] 268675 0
Baseline and 12 months after commencing intervention to assess intervention effects, then at 24 months after intervention commencement to assess maintenance.
Secondary outcome [10] 268676 0
10. Demographics and socio-economic status. A questionnaire will obtain demographic information e.g. age, ethnicity, marital status, language spoken at home, income and postcode
Timepoint [10] 268676 0
Measured at baseline
Secondary outcome [11] 268677 0
11. A process evaluation will be performed with a questionnaire to participants examining issues including study feasibility, participant satisfaction and suggestions for improvement.
Timepoint [11] 268677 0
measured 12 months after commencing intervention

Eligibility
Key inclusion criteria
Inclusion Criteria:
1. women 44 to 50 years of age
2. have had a menstrual period in the preceding 3 months
3. able to attend appointments in Newcastle
4. baseline Body Mass Index 18.5 to 29.9kg/m2
5. Women who have not had a hysterectomy or oophorectomy
6. Women without seriously medical conditions such as heart disease, Type 1 and 2 diabetes
7. Not pregnant
8. Women who can read write and understand English
Minimum age
44 Years
Maximum age
50 Years
Sex
Females
Can healthy volunteers participate?
Yes
Key exclusion criteria
1. Males
2. women no longer experiencing periods
3. women younger than 44 or older than 50 years of age
4. women who have had a hysterectomy
5. Women with Body Mass Index (BMI) of less than18.5 kg/m2 (Underweight) or above 29.9 kg/m2 (Obese). The rationale for these exclusions are based on incompatible goals i.e. the underweight need to gain weight, rather than prevent weight gain, while the obese need to lose at least 10% of body weight, which is outside the scope of the modest weight loss goals for the overweight women (7% or less).

Study design
Purpose of the study
Prevention
Allocation to intervention
Randomised controlled trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
54 women will be recruited by advertising via the University media Unit through radio, TV, newspapers, University Website and online media. After confirming they meet eligibility criteria, potential participants will be provided with a written Information Statement about the study to read prior to signing a consent form.

Once recruited, women attend the University for the baseline measures detailed in questions 12 and 13. The random number sequence generated by the statistician (see next point) were printed on sheets of paper, and numbers were allocated by CI1 as each participant registered to attend the baseline measures. Only one researcher (the Intervention Dietitian) had a copy of the key to which numbers were intervention and which were control. After the baseline measures the intervention Dietitian contacts the women by telephone to reveal their allocation. Only the dietitian completing the intervention appointments is aware of the allocation condition, and all researchers are unaware of the allocation at the time of the baseline measurements.
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Subjects will be randomly allocated to one of two groups using a randomised block design. The random allocation sequence has been generated by the study statistician, using a computer-based random number-producing algorithm in block lengths of six to ensure an equal chance of allocation to each group. Randomisation will be done with the Plan procedure ( Proc Plan) in the SAS statistical software package. The numbers are allocated as described above.
Masking / blinding
Blinded (masking used)
Who is / are masked / blinded?



Intervention assignment
Parallel
Other design features
Phase
Not Applicable
Type of endpoint/s
Efficacy
Statistical methods / analysis
Sample Size: The sample size calculation was based on the main outcome measure of body weight. Observational studies of women in this age group in the Australian population have demonstrated a mean (SD) weight gain of 1.04 (4.7) kg over a two-year period. Given both intervention groups were comprised of equal numbers of healthy weight and overweight women and presuming the overweight women would meet the intervention goal of losing 5 kg in the first 12 months and the healthy weight women would show zero weight change, the net weight change should be a 2.5 kg weight loss in the MI group by the end of phase 1. Based on the Australian data of net weight gain in the general population of mid-age women managing their weight by self-directed means [Williams et al, IJO; 2007, 31(6)978-986] we would expect a mean (SD) net weight gain of 0.5 (4.7) kg per year in our SDI (control) group. This would give an expected difference between the two groups of 3.0 kg after 12 months (end phase 1) and 3.5 kg after 24 months (end phase 2). Assuming equal sample sizes, to detect a difference in weight between groups of 3.5 kg with 80% power and a significance level of 0.05, a sample size of 22 women was required for each group. Allowing for an attrition rate of 20% by the end of 24 months, a total sample size of 55 women is required.
Statistical analyses
Outcome measures collected at baseline will be compared to those at 12 months (after adjusting for baseline weight) to assess intervention effects and compared with measures at 24 months (end phase 2) to assess whether the intervention effects were maintained. Analyses will be conducted using the intention to treat principle, and performed using SPSS version 19 (IBM). All variables will be checked for plausibility. Continuous variables will be assessed for normality. Independent sample t-tests and chi-squared tests will be conducted on continuous and categorical variables (respectively) to check they do not vary by intervention group at baseline, and by completers versus attriters. Analysis of covariance will be used to examine whether the intervention groups differed significantly in weight at each of 12 and 24 months after adjusting for baseline weight. Behaviour changes in diet and physical activity will be assessed as secondary outcome measures using analysis of covariance to determine whether the MI and SDI groups differed significantly in dietary or physical activity behaviours at 12 months. Results will be stratified for baseline BMI category.
Logistic regression analysis will be performed to assess whether categorical variables, such as smoking status significantly influenced weight. The visceral adipose tissue variable will be assessed for between group differences at 12 and 24 months using independent sample t-tests, and analyses stratified by BMI category to determine whether the results differed for the healthy weight and overweight women. Sensitivity analyses will be conducted to determine the effects on the outcomes of different methods of treating loss to follow-up (last observation carried forward versus imputation). The relationship between weight outcomes and compliance with the diet and physical activity behaviours will be assessed using mediation analysis [55].
A per protocol analysis will be conducted on women who adhered to the requirements of their assigned group. Adherent women are defined as those who completed all required eating and physical activity diaries over the 12-month period and attended all assessment sessions, regardless of assigned group, and who attended all five health professional consultations for the MI group. Results of the protocol adherent group will be compared with non-adherers in each group, that is, those who did not meet the adherence recommendations.

Recruitment
Recruitment status
Completed
Date of first participant enrolment
Anticipated
25/05/2010
Actual
25/05/2010
Date of last participant enrolment
Anticipated
Actual
29/06/2010
Date of last data collection
Anticipated
Actual
31/08/2012
Sample size
Target
54
Accrual to date
Final
54
Recruitment in Australia
Recruitment state(s)
NSW

Funding & Sponsors
Funding source category [1] 258223 0
University
Name [1] 258223 0
University of Newcastle
Country [1] 258223 0
Australia
Primary sponsor type
Individual
Name
Professor Lauren Williams, University of Canberra
Address
School of Health Sciences Faculty of Health University of Newcastle Callaghan NSW 2308
Country
Australia
Secondary sponsor category [1] 257390 0
Individual
Name [1] 257390 0
Professor Clare Collins
Address [1] 257390 0
School of Health Sciences
Faculty of Health
University of Newcastle
Callaghan
NSW 2308
Country [1] 257390 0
Australia
Secondary sponsor category [2] 257391 0
Individual
Name [2] 257391 0
Associate Professor Philip Morgan
Address [2] 257391 0
School of Education
Faculty of Education and Arts
University of Newcastle
Callaghan
NSW 2308
Country [2] 257391 0
Australia

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 260205 0
University of Newcastle Human Research Ethics Committee
Ethics committee address [1] 260205 0
Ethics committee country [1] 260205 0
Australia
Date submitted for ethics approval [1] 260205 0
Approval date [1] 260205 0
14/04/2010
Ethics approval number [1] 260205 0
H- 2010-0030

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

Contacts
Principal investigator
Name 32022 0
Prof Lauren Williams
Address 32022 0
Nutrition and Dietetics
Level 2, G40 Building
Griffith University
Gold Coast Campus
Parkville QLD 4222.
Country 32022 0
Australia
Phone 32022 0
+61 417028371
Fax 32022 0
Email 32022 0
[email protected]
Contact person for public queries
Name 15269 0
Prof Lauren Williams
Address 15269 0
School of Health Sciences
Griffith University
QLD 4222
Country 15269 0
Australia
Phone 15269 0
+61 7 56780155
Fax 15269 0
+61 2 4921 7053
Email 15269 0
[email protected]
Contact person for scientific queries
Name 6197 0
Prof Lauren Williams
Address 6197 0
as above
Country 6197 0
Australia
Phone 6197 0
+61 2 6206 8709
Fax 6197 0
+61 2 4921 7053
Email 6197 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
SourceTitleYear of PublicationDOI
EmbaseCan a relatively low-intensity intervention by health professionals prevent weight gain in mid-age women? 12-month outcomes of the 40-something randomised controlled trial.2014https://dx.doi.org/10.1038/nutd.2014.12
EmbaseMaintaining the outcomes of a successful weight gain prevention intervention in mid-age women: Two year results from the 40-something randomized control trial.2019https://dx.doi.org/10.3390/nu11051100
N.B. These documents automatically identified may not have been verified by the study sponsor.