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PRAMS: Peer-support To Reduce Antenatal Maternal Smoking

PRAMS: Peer-support To Reduce Antenatal Maternal Smoking: Development And Feasibility Testing Of A Social Media Group To Provide Peer Support And Enhance Quit Rates For Women Who Smoke In Pregnancy

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06595199
Acronym
PRAMS
Enrollment
72
Registered
2024-09-19
Start date
2024-10-31
Completion date
2025-10-31
Last updated
2024-09-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pregnancy Related, Smoking Cessation

Brief summary

The goal of this feasibility is test the feasibility of conducting a randomised trial of the use of an online peer support group to promote smoking cessation and enhance sustained abstinence for women who smoke in pregnancy. Researchers will compare the group who receive the intervention (along side standard care) with a group who receive standard care alone.

Detailed description

Participants will be asked to complete 2 questionnaires (and the intervention group will be asked to sign up to an online support group). They will be offered the opportunity to also take part in a follow up interview to explore acceptability and feasibility of the a future trial

Interventions

A closed online peer support group

Sponsors

University of Huddersfield
CollaboratorOTHER
National Institute for Health Research, United Kingdom
CollaboratorOTHER_GOV
The Leeds Teaching Hospitals NHS Trust
CollaboratorOTHER
King's College London
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Age
16 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Pregnant * Smoking at beginning of pregnancy * Access to mobile phone

Exclusion criteria

* Under 16 years of age

Design outcomes

Primary

MeasureTime frameDescription
Recruitment rate12 monthsNumber of participants as % of smokers booked at the Trust
Attrition rate12 monthsHow many participants complete all elements of the study

Secondary

MeasureTime frameDescription
Smoking status at end of pregnancy12 monthsSmoking status at end of pregnancy assessed by self report and cotinine testing
Engagement with stop smoking services12 monthsRecord of initial and subsequent visits

Contacts

Primary ContactTomasina Stacey, PhD
tomasina.stacey@kcl.ac.uk07580345393
Backup ContactHonor Morris
PRAMS@kcl.ac.uk

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026