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Improving Muslim Women's Uptake of Cancer Screening (IMCAN)

NCT06106165 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 200

Last updated 2025-04-16

No results posted yet for this study

Summary

The goal of this non-randomised trial is to test how a workshop that includes religiously-tailored messages can help increase the uptake of breast, colorectal and cervical cancer screening among Muslim women in North East England and Scotland.

The results of this trial will inform the development of a full-scale randomised-controlled trial.

Participants in this study will be asked to take part in a two-hour workshop, deliver either online or in-person.

Conditions

Interventions

OTHER

In-person peer-led faith-based intervention to encourage breast, bowel, and cervical screening uptake among Muslim women

The intervention includes a two-hour workshop, delivered in-person, that aims to improve the uptake of cancer screening among Muslim women. The workshop consists of four parts: * A peer-led discussion on barriers and facilitators to breast, cervical and colorectal cancer screening * A health information session led by a health professional * Videos of Muslim women talking about their experiences with cancer screening * A religious perspective on cancer screening led by a female religious scholar

OTHER

Online In-person peer-led faith-based intervention to encourage breast, bowel, and cervical screening uptake among Muslim women

The intervention includes a two-hour workshop, delivered online, that aims to improve the uptake of cancer screening among Muslim women. The workshop consists of four parts: * A peer-led discussion on barriers and facilitators to breast, cervical and colorectal cancer screening * A health information session led by a health professional * Videos of Muslim women talking about their experiences with cancer screening * A religious perspective on cancer screening led by a female religious scholar

Sponsors & Collaborators

  • University of Glasgow

    collaborator OTHER

  • University of Sunderland

    lead OTHER

Study Design

Allocation
NON_RANDOMIZED
Purpose
OTHER
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
25 Years
Max Age
74 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2023-11-01
Primary Completion
2025-10-31
Completion
2025-12-31

Countries

  • United Kingdom

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06106165 on ClinicalTrials.gov