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

Status Recruiting

Clinical Trial 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.

Clinical Trial Description

Low rates of cancer screening among Muslim women puts them at higher risk of death from screening since they do not detect cancer early. This study will work to increase the uptake of cancer screening among Muslim women using two-hour workshops delivered in the community. The workshops were developed with the help of 10 Muslim women in Scotland. The workshops include four parts: - A discussion on the barriers and facilitators to breast, cervical and colorectal cancer screening - A health information session given by a female health provider on cancer screening - Videos of Muslim women talking about their experiences with cancer screening - A session given by a female religious scholar to discuss Islamic perspectives on cancer screening. Another eighteen Muslim women then took part in the workshops; they gave positive feedback on the content of the workshops and how the sessions were delivered. In the feasibility trial, the workshops will be delivered to 200 Muslim women to find out whether a full-scale randomised-controlled trial can take place. This study will be carried out with the help of 10 Muslim women who will give advice on the content of the workshops and plan for implementation; they will also help with the delivery of the workshops. It is expected that this study will lead to changes in knowledge and screening uptake among participants. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT06106165
Study type	Interventional
Source	University of Sunderland
Contact	Floor Christie-de Jong
Phone	0191 5153445
Email	floor.christie@sunderland.ac.uk
Status	Recruiting
Phase	N/A
Start date	November 1, 2023
Completion date	December 2025

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Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.

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

Clinical Trial Summary

Clinical Trial Description

Study Design

Related Conditions & MeSH terms