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Evaluation of an Educational Intervention for Women With Breast Pain

Primary Purpose

Breast Pain, Mastalgia

Status
Unknown status
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Breast Pain video
Semi-structure interviews
Sponsored by
Royal Marsden NHS Foundation Trust
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Breast Pain

Eligibility Criteria

18 Years - 40 Years (Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

  • Healthy female patients aged between 18 years and 40 years on the day of clinic attendance (referred to one-stop breast clinic with breast pain alone)
  • Normal examination in clinic
  • No further breast investigations undertaken or required

Exclusion Criteria:

  • Presence of concerning features during clinical examination requiring further investigation
  • Pregnancy or lactation at the time of study diagnosis.
  • Strong family history of breast cancer
  • Recent previous imaging or clinic attendance for same symptom within last 12 months
  • Previous history of breast cancer
  • Current or previous treatment with Tamoxifen
  • Medical or psychiatric illness which, in the opinion of the assessing clinician, might impact their participation in the study

Sites / Locations

  • Royal Marsden Hospital NHS Foundation Trust

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Single Arm

Arm Description

Eligible patients who are referred to the "one-stop" diagnostic clinic with breast pain alone and have completed a clinical assessment will be given a patient information sheet inviting them to participate in the study. They will be met by the interviewing clinician at the same visit.

Outcomes

Primary Outcome Measures

Patient's perceptions on the breast-pain video
Due to the semi-structure interview qualitative nature of the study the primary objective is to obtain observational data for insights and patterns (through "quotes") of women's perceptions of an educational video about breast pain, breast awareness and self-examination and its impact on their confidence in self-management of breast pain.

Secondary Outcome Measures

Video's purpose evaluation
proportion of women who report that the video Was informative Might have reassured them enough not to have needed to seek an appointment in secondary care

Full Information

First Posted
April 18, 2019
Last Updated
May 2, 2019
Sponsor
Royal Marsden NHS Foundation Trust
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1. Study Identification

Unique Protocol Identification Number
NCT03936842
Brief Title
Evaluation of an Educational Intervention for Women With Breast Pain
Official Title
Evaluation of an Educational Intervention for Women With Breast Pain
Study Type
Interventional

2. Study Status

Record Verification Date
May 2019
Overall Recruitment Status
Unknown status
Study Start Date
May 31, 2019 (Anticipated)
Primary Completion Date
July 31, 2019 (Anticipated)
Study Completion Date
September 30, 2019 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Royal Marsden NHS Foundation Trust

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Evaluation of an educational intervention for women with breast pain Target Problem -Symptomatic breast pain Study Objectives- The primary objective is to obtain knowledge of women's perceptions of an educational video about breast pain, breast awareness and self-examination and its impact on their confidence in self-management of breast pain. The secondary objectives -proportion of women who report that the video Was informative Might have reassured them enough not to have needed to seek an appointment in secondary care. Study Design- Prospective single-centre mixed methods study through semi-structured interviews for Masters in Public Health thesis Trial Population -Women, aged 18-40, referred to "one-stop" / rapid diagnostic breast clinic at The Royal Marsden Hospital (RMH) with breast pain alone. Recruitment target Until saturation, expected sample 10-15 Trial Design- Mixed methods study using semi-structured interviews Primary endpoint -This is a qualitative study, with no statistical primary end point. Secondary endpoints-Descriptive summaries of two questions will be reported as a secondary end point. Inclusion Criteria Women aged between 18 years and 40 years on the day of clinic attendance Breast pain as the only symptom Normal clinical examination No further investigation (imaging, biopsy etc) Exclusion Criteria Presence of suspicious features during clinical examination requiring further investigation Strong family history of breast cancer Previous breast imaging within last 12 months Previous history of breast cancer Current or previous treatment with Tamoxifen Concurrent cancer Medical or psychiatric illness which might impact their participation in the study
Detailed Description
The prevalence of breast pain has been reported to be between 41-69% in clinical cohorts and in the general population (1-4). The incidence of cancer in women with breast pain alone (ie no lump or other, more concerning symptoms) is low, with published rates between 1 to 1.8% (7-9). Furthermore, the prevalence of breast pain increases linearly up to the age of 50 and then decreases (4), thus women under 40 with a normal clinical examination do not require further investigations and can be reassured in primary care. Despite this, mastalgia is one of the most common symptoms in women referred to a breast unit representing up to 69% of attendances (5-7). Consequently, women affected by breast pain are up to 4.7 times more likely to have had a mammogram than asymptomatic women (6). ln order to facilitate early breast cancer diagnosis there is a suspected cancer pathway referral (for an appointment within 2 weeks) from primary care to specialist units. Recent increases in breast urgent referrals have increased the pressure on already overstretched services. Many strategies have been tried to manage the tension between the desire for early detection of breast cancer, and avoiding unnecessary referral for normal breast sensations. Although breast screening by self-examination or clinical examination has not been shown to reduce breast cancer mortality in studies (10), breast awareness can be linked to early detection that facilitates treatment and has the potential to reduce mortality (11). Therefore, breast awareness and self-examination have become relevant parts of general breast education promoting women's confidence to discern between normality and unusual changes (12-17). Self-examination is not frequently taught in primary care and "there is a need to develop more innovative strategies to promote breast health awareness and early detection of breast cancer in women" (18). In this study, as part of a Masters in Health Policy, we are investigating the impact of an educational video, here to be shown after a clinic appointment, but with the potential to be distributed to general practitioners, and to patients directly if favourably received. Methodology Patient recruitment 1.1 Initial visit to "one-stop"clinic Eligible patients who are referred to the "one-stop" diagnostic clinic with breast pain alone and have completed a clinical assessment will be given a patient information sheet inviting them to participate in the study. They will be met by the interviewing clinician at the same visit. 1.2 Consent Consent will be sought by the clinician who will undertake the interviews. Intervention: educational video An educational video of approximately 10 minutes about breast pain, self-examination and breast awareness will be shown to the participant. Semi-structured interview A semi-structured, face-to-face interview will be then undertaken. The principles of Grounded Theory will be used to guide the interview. All of the interviews will be recorded and transcribed securely, only referencing the patient according to their study number. Their name and hospital number will not be used. A number of pre-planned, open questions will be asked. The core questions are related to the topic of discussion - impressions related to the intervention and subsequent effect into their previous concerns. Further questions will evolve in response to answers given by earlier participants. The duration of the interview will depend on the extent of the answers and any follow-up questions that derive later from earlier answers. Data Acquisition and analysis The video show and interview will be undertaken in a private room after routine clinical assessment. The interviewer will be the MSc student, a medically-qualified breast clinician with an interest in breast pain, who has read the relevant literature. The recorded interview and notes taken by investigator during the interview are the only data. The analysis will run alongside data collection as an iterative process to inform further sampling. The purpose of the analysis is to describe the participants' opinion and to develop theoretical explanations for these. The interviews will be analysed by reading the transcripts in detail and assigning codes to give meaning to segments of the text. Emerging codes will be grouped into themes and discussed and then explored in subsequent interviews. The analysis will be undertaken using the constant comparison technique of grounded theory whereby data will be examined for differences and similarities within the themes, taking into account the patient context. The initial codes will be modified and new codes added as the project progresses. New data will be compared with previous interviews to identify the similarities and differences. Evaluation of Outcome This is a mixed methods study. As a result, we will have increased knowledge of the perceptions of women presenting with breast pain about an educational video. We will have some quantitative information about whether they find it informative and whether it might lead them to avoid attending secondary care. It will guide the future management of women with pain at the interface of primary and secondary care.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Pain, Mastalgia

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
15 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Single Arm
Arm Type
Experimental
Arm Description
Eligible patients who are referred to the "one-stop" diagnostic clinic with breast pain alone and have completed a clinical assessment will be given a patient information sheet inviting them to participate in the study. They will be met by the interviewing clinician at the same visit.
Intervention Type
Behavioral
Intervention Name(s)
Breast Pain video
Intervention Description
An educational video of approximately 10 minutes about breast pain, self-examination and breast awareness will be shown to the participant.
Intervention Type
Behavioral
Intervention Name(s)
Semi-structure interviews
Intervention Description
A semi-structured, face-to-face interview will be then undertaken. The principles of Grounded Theory will be used to guide the interview. All of the interviews will be recorded and transcribed securely, only referencing the patient according to their study number. Their name and hospital number will not be used.
Primary Outcome Measure Information:
Title
Patient's perceptions on the breast-pain video
Description
Due to the semi-structure interview qualitative nature of the study the primary objective is to obtain observational data for insights and patterns (through "quotes") of women's perceptions of an educational video about breast pain, breast awareness and self-examination and its impact on their confidence in self-management of breast pain.
Time Frame
10 minutes
Secondary Outcome Measure Information:
Title
Video's purpose evaluation
Description
proportion of women who report that the video Was informative Might have reassured them enough not to have needed to seek an appointment in secondary care
Time Frame
10 minutes

10. Eligibility

Sex
Female
Gender Based
Yes
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
40 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Healthy female patients aged between 18 years and 40 years on the day of clinic attendance (referred to one-stop breast clinic with breast pain alone) Normal examination in clinic No further breast investigations undertaken or required Exclusion Criteria: Presence of concerning features during clinical examination requiring further investigation Pregnancy or lactation at the time of study diagnosis. Strong family history of breast cancer Recent previous imaging or clinic attendance for same symptom within last 12 months Previous history of breast cancer Current or previous treatment with Tamoxifen Medical or psychiatric illness which, in the opinion of the assessing clinician, might impact their participation in the study
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Ann Gandolfi
Phone
02086613903
Email
ann.gandolfi@rmh.nhs.uk
First Name & Middle Initial & Last Name or Official Title & Degree
Jennifer Rusby, consultant
Phone
07957648248
Email
Jennifer.Rusby@rmh.nhs.uk
Facility Information:
Facility Name
Royal Marsden Hospital NHS Foundation Trust
City
London
ZIP/Postal Code
SW3 6JJ
Country
United Kingdom

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
Citation
Ader DN, Shriver CD. Update on clinical and research issues in cyclical mastalgia. Breast J 1998;4:25-32.
Results Reference
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3812845
Citation
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Results Reference
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PubMed Identifier
15008609
Citation
Smith RL, Pruthi S, Fitzpatrick LA. Evaluation and management of breast pain. Mayo Clin Proc. 2004 Mar;79(3):353-72. doi: 10.4065/79.3.353.
Results Reference
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PubMed Identifier
25041468
Citation
Scurr J, Hedger W, Morris P, Brown N. The prevalence, severity, and impact of breast pain in the general population. Breast J. 2014 Sep-Oct;20(5):508-13. doi: 10.1111/tbj.12305. Epub 2014 Jul 7.
Results Reference
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PubMed Identifier
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Citation
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Results Reference
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PubMed Identifier
9240595
Citation
Ader DN, Browne MW. Prevalence and impact of cyclic mastalgia in a United States clinic-based sample. Am J Obstet Gynecol. 1997 Jul;177(1):126-32. doi: 10.1016/s0002-9378(97)70450-2.
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PubMed Identifier
10215561
Citation
Barton MB, Elmore JG, Fletcher SW. Breast symptoms among women enrolled in a health maintenance organization: frequency, evaluation, and outcome. Ann Intern Med. 1999 Apr 20;130(8):651-7. doi: 10.7326/0003-4819-130-8-199904200-00005.
Results Reference
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PubMed Identifier
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Citation
Eberl MM, Phillips RL Jr, Lamberts H, Okkes I, Mahoney MC. Characterizing breast symptoms in family practice. Ann Fam Med. 2008 Nov-Dec;6(6):528-33. doi: 10.1370/afm.905.
Results Reference
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PubMed Identifier
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Citation
Joyce DP, Alamiri J, Lowery AJ, Downey E, Ahmed A, McLaughlin R, Hill AD. Breast clinic referrals: can mastalgia be managed in primary care? Ir J Med Sci. 2014 Dec;183(4):639-42. doi: 10.1007/s11845-013-1066-z. Epub 2014 Jan 9.
Results Reference
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PubMed Identifier
12804462
Citation
Kosters JP, Gotzsche PC. Regular self-examination or clinical examination for early detection of breast cancer. Cochrane Database Syst Rev. 2003;2003(2):CD003373. doi: 10.1002/14651858.CD003373.
Results Reference
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Citation
Richards MA. The National Awareness and Early Diagnosis Initiative in England: assembling the evidence. Br J Cancer. 2009 Dec 3;101 Suppl 2(Suppl 2):S1-4. doi: 10.1038/sj.bjc.6605382.
Results Reference
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Citation
Mac Bride MB, Pruthi S, Bevers T. The evolution of breast self-examination to breast awareness. Breast J. 2012 Nov-Dec;18(6):641-3. doi: 10.1111/tbj.12023. Epub 2012 Sep 26. No abstract available.
Results Reference
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19273403
Citation
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Results Reference
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Links:
URL
https://www.nice.org.uk/guidance/cg164
Description
National Institute for Health and Clinical Excellence (NICE). Familial Breast Cancer: Full Guideline.
URL
http://screening.iarc.fr/breastselfexamination.php
Description
International Agency for Research on Cancer (IARC). IARC Screening Group.
URL
http://www.cancerscreening.nhs.uk/breastscreen/breastawareness.html
Description
National Office of NHS Cancer Screening Programmes, Public Health England. NHS Breast Cancer Screening Programme 2013

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Evaluation of an Educational Intervention for Women With Breast Pain

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