Effects of Expectations and Body Image in Breast Reconstruction

Sponsor
Vastra Gotaland Region (Other)
Overall Status
Recruiting
CT.gov ID
NCT04714463
Collaborator
(none)
500
1
46.9
10.6

Study Details

Study Description

Brief Summary

A breast reconstruction after mastectomy, either due to breast cancer or a high lifetime risk for cancer, is performed to increase the patient's quality of life. However, there are studies that show that some women regret their decision to have breast reconstruction. There are also studies demonstrating similarities in the general patterns of psychosocial adjustment and quality of life among women with breast cancer who have undergone breast-conserving surgery, mastectomy alone, and mastectomy combined with breast reconstruction. Hence, it is unclear which women actually benefit from a breast reconstruction. The concept of quality of life is connected to patient satisfaction and body image/investment. Therefore, the aim of this project is to examine the effects of patient expectations and body image on the patient reported outcomes of breast reconstruction, to improve preoperative information and postoperative care for women considering a breast reconstruction.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Implant-based breast reconstruction
  • Procedure: Autologous breast reconstruction
  • Procedure: Combined methods

Study Design

Study Type:
Observational
Anticipated Enrollment :
500 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Psychological Effect of Expectations and Body Image on Outcomes of Breast Reconstruction
Actual Study Start Date :
Feb 1, 2021
Anticipated Primary Completion Date :
Dec 31, 2023
Anticipated Study Completion Date :
Dec 31, 2024

Arms and Interventions

Arm Intervention/Treatment
Immediate breast reconstruction

Women undergoing immediate breast reconstruction due to breast cancer or a high risk for breast cancer

Procedure: Implant-based breast reconstruction
All types of implant based breast reconstructions

Procedure: Autologous breast reconstruction
All types of autologous breast reconstructions

Procedure: Combined methods
All types of breast reconstructions combining autologous and implant based techniques

Delayed breast reconstruction

Women undergoing delayed breast reconstruction due to breast cancer or a high risk for breast cancer

Procedure: Implant-based breast reconstruction
All types of implant based breast reconstructions

Procedure: Autologous breast reconstruction
All types of autologous breast reconstructions

Procedure: Combined methods
All types of breast reconstructions combining autologous and implant based techniques

Outcome Measures

Primary Outcome Measures

  1. Patient satisfaction with breast reconstruction measured with Breast Q reconstruction [2 years]

    Breast Q reconstruction includes two domains and six different modules: health-related quality of life (HR-QOL; including physical, psychosocial, and sexual well-being) and patient satisfaction (including satisfaction with breasts, outcome, and care). Each scale produces an independent score from 0-100. A higher score means greater satisfaction or better QOL.

  2. Patient expectations measured with Breast Q expectations [2 years]

    Breast Q expectations.The scale consists of five modules: expectations for support from medical staff , expectations for pain, expectations for coping, expectations for breast appearance when clothed and expectations for breast sensation. The score for each independent scale range from 0-100. A higher score means greater expectations.

  3. Body image measured with Multidimensional body-self relations questionnaire- appearance scales (MBSRQ-AS) [2 years]

    MBSRQ-AS - Multidimensional body-self relations questionnaire- appearance scales.It is a 34-item self-report questionnaire designed to measure appearance related components of body-image. In consists of five subscales: appearance evaluation, appearance orientation, body areas satisfaction, overweight preoccupation, and self-classified weight. It is a 5-point Likert-scale ranging from 1 to 5.

  4. Body image investment measured with Appearance schemas inventory-revised (ASI-R) [2 years]

    ASI-R - Appearance schemas inventory-revised: is a 20-item self-report questionnaire designed to measure body-image investment. It consists of two subscales, self-evaluative salience (SES) and motivational salience (MS). It is a 5-point Likert-scale ranging from 1 (strongly disagree) to 5 (strongly agree). Twelve items relate to SES and eight items relate to MS. The total score is the mean of the 20 items, and the score of the subscales is the mean of the items relating to each subscale. A high score indicates greater body-image investment.

Secondary Outcome Measures

  1. Satisfaction with preoperative information measured with Breast Q reconstruction [2 years]

    Measured with one of the sub scales of Breast Q reconstruction

  2. Pain measured with a visual analogue scale [2 weeks]

    Measured with a post-operative pain dairy with VAS scales (o means no pain and 10 means the worst possible pain imaginable)

  3. Sick leave according to authorities [1 year]

    Actual sick leave according to the Swedish authorities

  4. Number of out-patient visits according to the medical charts [1 year]

    Actual number of out-patient visits, according to the medical chart

  5. Depression and anxiety measured with Hospital Anxiety and Depression Scale (HADS) [2 years]

    HADS - Hospital Anxiety and Depression Scale: is a 14-item self-report questionnaire that is designed to measure anxiety and depression. It has two domains, where seven items relate to anxiety and seven relate to depression. It is a 4-point Likert-scale ranging from 0-3. Each domain has a maximum score of 21. For both domains, scores of less than 7 indicate non-cases, whereas scores of 8-10 indicate mild anxiety or depression, 11-14 moderate and 15-21 severe.

  6. Demographic factors and medical factors according to medical charts [2 years]

    Demographic factors that might affect expectations and satisfaction, such as age, comorbidity, and previous cosmetic breast surgery, and medical factors such as timing of reconstructions, reason for mastectomy, type of cancer and cancer treatment received.

Other Outcome Measures

  1. Translation and validation of Breast-Q expectations [4 months]

    Translation into Swedish according to MAPI-guidelines. Validation of psychometric properties in a Swedish population.The scale consists of five modules: expectations for support from medical staff , expectations for pain, expectations for coping, expectations for breast appearance when clothed and expectations for breast sensation. The score for each independent scale range from 0-100. A higher score means greater expectations.

  2. Translation and validation of Appearance schemas inventory-revised (ASI-R) [4 months]

    Translation into Swedish according to MAPI-guidelines. Validation of psychometric properties in a Swedish population. ASI-Ris a 20-item self-report questionnaire designed to measure body-image investment. It consists of two subscales, self-evaluative salience (SES) and motivational salience (MS). It is a 5-point Likert-scale ranging from 1 (strongly disagree) to 5 (strongly agree). Twelve items relate to SES and eight items relate to MS. The total score is the mean of the 20 items, and the score of the subscales is the mean of the items relating to each subscale. A high score indicates greater body-image investment.

  3. Translation and validation of Multidimensional body-self relations questionnaire- appearance scales (MBSRQ-AS) [4 months]

    Translation into Swedish according to MAPI-guidelines. Validation of psychometric properties in a Swedish population.Multidimensional body-self relations questionnaire- appearance scales.It is a 34-item self-report questionnaire designed to measure appearance related components of body-image. In consists of five subscales: appearance evaluation, appearance orientation, body areas satisfaction, overweight preoccupation, and self-classified weight. It is a 5-point Likert-scale ranging from 1 to 5.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Biological women with breast cancer or high risk for breast cancer who want post-mastectomy breast reconstruction

  • Age > 18 years

Exclusion Criteria:
  • Inability to give informed consent

  • Inability to understand Swedish

  • Relaps of cancer

  • Palliative treatment

Contacts and Locations

Locations

Site City State Country Postal Code
1 Sahlgrenska university hospital Gothenburg Sweden 413 45

Sponsors and Collaborators

  • Vastra Gotaland Region

Investigators

  • Principal Investigator: Emma Hansson, PhD, Göteborg University

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Vastra Gotaland Region
ClinicalTrials.gov Identifier:
NCT04714463
Other Study ID Numbers:
  • 2020-06245
First Posted:
Jan 19, 2021
Last Update Posted:
May 3, 2022
Last Verified:
Apr 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Vastra Gotaland Region

Study Results

No Results Posted as of May 3, 2022