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Trial registered on ANZCTR
Registration number
ACTRN12625000715471
Ethics application status
Approved
Date submitted
5/06/2025
Date registered
7/07/2025
Date last updated
7/07/2025
Date data sharing statement initially provided
7/07/2025
Type of registration
Prospectively registered
Titles & IDs
Public title
A culturally-tailored physical activity intervention for mothers and their adolescent daughters: Ummah Moves
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Scientific title
The feasibility and acceptability of a culturally tailored mother-daughter physical activity intervention: Ummah Moves.
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Secondary ID [1]
314459
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Nil
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Universal Trial Number (UTN)
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Trial acronym
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Linked study record
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Health condition
Health condition(s) or problem(s) studied:
Physical inactivity
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Condition category
Condition code
Public Health
333859
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0
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Health promotion/education
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Intervention/exposure
Study type
Interventional
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Description of intervention(s) / exposure
The study is designed to test the feasibility and acceptability of a culturally-tailored physical activity intervention for mothers and their adolescent daughters from a Middle Eastern background and of Islamic faith. To ensure that this intervention is culturally appropriate and acceptable for this population, the culturally-tailoring process of this intervention was informed by formative research and input from key stakeholders (i.e., a community liaison officer, chief project officer, personal trainer, and a mother adolescent daughter duo) of a similar cultural background.
Participants (mothers and their adolescent daughters) will attend 8 face-to-face group-based sessions scheduled on a weekly basis. Each session will last 90 minutes in duration and include educational and practical physical activity sessions. Educational sessions for the intervention will be conducted with the whole group and will include a combination of lectures, group discussions, and mother-daughter partner activities. Topics covered will include: an overview of physical activity (e.g., definition, benefits, recommended guidelines), navigating cultural expectations, barriers and facilitators, social perceptions (e.g., around modesty), muscle strengthening activities, family and community support. The physical activity sessions will include activities with the whole group (e.g., Zumba) and smaller partner activities (e.g., circuit training, body weight exercises). The activities will be of moderate-vigorous intensity accommodating to all fitness and skill levels and will include culturally-relevant forms of physical activity.
The intervention will take place at Amity College Prestons campus (Sydney, Australia) and the sessions will be facilitated by a PhD candidate, who is a Masters-level qualified Health and Physical Education teacher. Each session will target a maximum of 30 mother–daughter dyads (a maximum of 60 participants in total). Adherence to the intervention will be monitored using session attendance checklists.
Semi-structured focus groups will be conducted to explore participants’ experiences with the program, focusing on its acceptability, perceived challenges, facilitators to participation, and suggestions for improvement. Separate groups will be held for daughters and mothers to allow for open and comfortable discussions. Open-ended questions from the process evaluation questionnaire will further capture detailed participant feedback.
Mothers and daughters enrolled in the intervention will be invited to participate. A maximum of 30 mothers and 30 daughters may be invited, with individual focus groups capped at approximately 8–10 participants each. The focus groups will be conducted by the principal investigator and trained female research assistants. All participants will be invited to take part. There will be no selection criteria or exclusion; participation will be open to all who express interest.
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Intervention code [1]
331080
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Lifestyle
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Intervention code [2]
331081
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Behaviour
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Comparator / control treatment
No control group
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Control group
Uncontrolled
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Outcomes
Primary outcome [1]
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Recruitment rates
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Assessment method [1]
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Recruitment will be assessed by analysing study enrolment data, with a target of approximately 30 mother-daughter dyads. Data will be audited using a recruitment tracking sheet.
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Timepoint [1]
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Immediately post-program (8 weeks)
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Primary outcome [2]
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Acceptability of the intervention among mothers.
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Assessment method [2]
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Acceptability of the intervention will be explored through semi-structured focus groups conducted with mothers. The focus groups will be facilitated by a trained female research assistant with experience in conducting focus groups. Discussions will explore mothers’ perceptions of the intervention’s content, cultural relevance, delivery format, and overall experience.
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Timepoint [2]
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Immediately post-intervention (8 weeks)
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Primary outcome [3]
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Program satisfaction
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Assessment method [3]
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Program satisfaction will be measured via a 4-point Likert scale questionnaire, with a target satisfaction rate of ~80%.
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Timepoint [3]
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Immediately post-intervention (8 weeks)
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Secondary outcome [1]
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Physical activity
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Assessment method [1]
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Compliance with wearing the accelerometer to be measured using Actigraph GT3x. Participants will be asked to wear an accelerometer for 7 days. A valid week is typically defined as having at least 4 valid days of data, with at least one of those days being a weekend. A day is considered valid if the accelerometer is worn for a minimum number of at least 10 hours of wear time during waking hours.
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Timepoint [1]
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Baseline, post-intervention (8 weeks)
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Secondary outcome [2]
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Session attendance
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Assessment method [2]
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Session attendance will be assessed through weekly attendance records. The target will be at least 70% of participants (mothers and their adolescent daughter) attendance over the 8-week period.
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Timepoint [2]
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Ongoing throughout the intervention.
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Secondary outcome [3]
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Retention rates (Primary outcome)
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Assessment method [3]
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Retention will be assessed based on the number of participants who complete the program with a predefined benchmark of at least 80%.
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Timepoint [3]
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Immediately post-program (8 weeks)
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Secondary outcome [4]
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Acceptability of the intervention among adolescent daughters (Primary outcome)
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Assessment method [4]
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Acceptability of the intervention will be explored through semi-structured focus groups conducted with daughters. The focus groups will be facilitated by a trained female research assistant with experience in conducting focus groups. Discussions will explore daughters’ perceptions of the intervention’s content, cultural relevance, delivery format, and overall experience.
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Timepoint [4]
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Immediately post-intervention (8 weeks)
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Eligibility
Key inclusion criteria
This study will be recruiting mother-daughter dyads.
Mother/ Female caregivers:
- Willing and able to attend a physical activity program at Amity College Prestons Campus for an 8-week period (including baseline and end of intervention data collection)
- From a Middle Eastern background
- From an Islamic faith
- Have a female child aged 12-15 years
- Mother/ female caregiver must also be capable of partaking in moderate-intensity physical activity.
Adolescent Girls:
- Willing and able to attend a physical activity program at Amity College Prestons Campus for a 8-weeks period (including baseline and end of intervention data collection)
- From a Middle Eastern background
- From an Islamic faith
- Have a mother/ female caregiver willing to participate in the program.
- Adolescent and female adult participant must also be capable of partaking in moderate-intensity physical activity.
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Minimum age
12
Years
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Maximum age
64
Years
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Sex
Females
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Can healthy volunteers participate?
Yes
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Key exclusion criteria
Participants who cannot participate in moderate intensity physical activity, not willing to commute to the location, or have a physical or intellectual disability and have not been cleared by a GP to participate in the program, will be excluded.
Further, participants who do not pass the pre-exercise health screening questionnaire and do not provide GP clearance will be excluded from participating in physical activity.
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Study design
Purpose of the study
Prevention
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Allocation to intervention
Non-randomised trial
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Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
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Methods used to generate the sequence in which subjects will be randomised (sequence generation)
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Masking / blinding
Open (masking not used)
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Who is / are masked / blinded?
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Intervention assignment
Single group
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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
7/07/2025
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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
30
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Accrual to date
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Final
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Recruitment in Australia
Recruitment state(s)
NSW
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Funding & Sponsors
Funding source category [1]
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University
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Name [1]
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Western Sydney University
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Address [1]
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Country [1]
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Australia
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Primary sponsor type
University
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Name
Western Sydney University
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Address
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Country
Australia
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Secondary sponsor category [1]
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None
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Name [1]
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Address [1]
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Country [1]
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Ethics approval
Ethics application status
Approved
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Ethics committee name [1]
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University of Western Sydney Human Research Ethics Committee
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Ethics committee address [1]
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https://www.westernsydney.edu.au/research/research_ethics_and_integrity/human_ethics/apply_for_human_research_ethics_review
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Ethics committee country [1]
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Australia
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Date submitted for ethics approval [1]
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30/01/2025
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Approval date [1]
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26/06/2025
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Ethics approval number [1]
317610
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Summary
Brief summary
To our knowledge, there are no known scientifically evaluated physical activity interventions designed for mothers and daughters from a Middle Eastern background and of an Islamic faith. While several physical activity interventions for mother–daughter dyads exist, none have been specifically tailored for Middle Eastern and Muslim families, an important gap given the distinct cultural and religious influences on women's and girls’ physical activity in these communities. The aim of this study is to assess the feasibility and acceptability of an 8-week culturally adapted physical activity program for mothers and their daughters from a Middle Eastern and Islamic background
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Trial website
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Trial related presentations / publications
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Public notes
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Contacts
Principal investigator
Name
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Ms Nariman Dennaoui
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Address
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Western Sydney University, School of Health Sciences, Locked Bag 1797 Penrith NSW 2751
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Country
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Australia
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Phone
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+61 2 4736 0052
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Fax
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Email
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[email protected]
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Contact person for public queries
Name
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Associate Professor Emma George
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Address
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Western Sydney University, School of Health Sciences, Locked Bag 1797 Penrith NSW 2751
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Country
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Australia
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Phone
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+61 2 4736 0052
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Fax
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Email
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[email protected]
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Contact person for scientific queries
Name
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Associate Professor Emma George
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Address
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Western Sydney University, School of Health Sciences, Locked Bag 1797 Penrith NSW 2751
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Country
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Australia
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Phone
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+61 2 4736 0052
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Fax
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Email
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[email protected]
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Data sharing statement
Will the study consider sharing individual participant data?
No
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.
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