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Breast ReconstructionNCT07355946

The Effect of Nurse-Led Coaching Program on Self-Care Agency and Quality of Life in Reconstructed Breast Cancer Patients

A study testing Nurse-led Coaching Program in people with Breast Reconstruction, run by Gazi University at 1 site in Turkey (Türkiye).

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The primary objective of this clinical study is to examine the effects of a nurse-led coaching program on self-care agency and quality of life in patients who have undergone reconstructive surgery for breast cancer. 1. Read more about this study

Who is it for?
Any age, women only
Conditions the study is for
Breast Reconstruction
What is being tested?
Nurse-led Coaching Program
Could I receive a placebo?
No, everyone receives an active treatment
How many people
58 participants
Where
1 siteTurkey (Türkiye)
Study dates
24 Feb 2025to 1 Dec 2025
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages Any age
  • Women only
  • No healthy volunteers
  • Child, Adult, Older adult

Who may be able to join

  • Having undergone breast reconstruction surgery due to breast cancer,
  • Being 18 years of age or older,
  • Being able to understand and speak Turkish,
  • Voluntarily agreeing to participate in the study,
  • Being able to read and write.

Who cannot join

  • Having a speech, hearing, or vision impairment,
  • Having a psychiatric diagnosis or ongoing treatment,
  • Having metastatic breast cancer,
  • Having a cancer diagnosis other than breast cancer.

Trial locations and contacts

1 site in 1 country.

Turkey (Türkiye)1 site
  • Gazi University Health, Research and Application Center

    Ankara, Ankara, 06560

Other trials in Turkey (Türkiye)

About this study

The primary objective of this clinical study is to examine the effects of a nurse-led coaching program on self-care agency and quality of life in patients who have undergone reconstructive surgery for breast cancer.

  1. Is there a difference in self-care agency between breast reconstructive patients who received a nurse-led coaching program and those who did not?
  2. Is there a difference in quality of life between breast reconstructive patients who received a nurse-led coaching program and those who did not? The secondary objective of this clinical study is to determine the satisfaction levels of patients who participated in a nurse-led coaching program for breast reconstructive surgery. The secondary questions the study aims to answer are:
  3. What is the satisfaction level of breast reconstructive patients who received a nurse-led coaching program?
Read more

The researchers will compare whether there are differences in self-care agency and quality of life between breast cancer patients who received a nurse-led coaching program (intervention group) and those who did not (control group).

Participants:

  • Patients who meet the inclusion criteria will be informed of the study's purpose during their postoperative hospital stay, and their informed consent will be obtained. Patients who agree to participate will complete an Introductory Information Form, the Self-Care Agency Scale, and the EORTC QLQ-C30 and QLQ-BR-42 Quality of Life Scales.
  • After completing the pre-test measurements, the researchers will randomly assign patients to either the control or intervention groups using a random number table.
  • Patients in the intervention group will receive a routine debriefing on the day of discharge and a total of nine coaching sessions, scheduled weekly for the first 6 weeks and biweekly for the following 6 weeks. These sessions will be conducted via online meeting.
  • Patients in the control group will receive a routine debriefing only on the day of discharge.
  • Post-test measurements will be administered to both groups at 12 weeks post-operatively.
Read the detailed description

MATERIALS AND METHODS

  1. Research Method This study was planned as a randomized controlled experimental study to determine the effects of a nurse-led coaching program on self-care agency and quality of life in breast cancer patients undergoing reconstruction.
  2. Location and Characteristics of the Study The study is being conducted in 2025 at the Gazi University Health Research and Application Center (GUSAUM) Plastic Reconstructive and Hand Surgery Clinic and the Ankara Etlik City Hospital Plastic Surgery Clinic at Türkiye. In these clinics, breast reconstruction surgeries are performed simultaneously with breast cancer surgery, and in the early and late postoperative periods. Patients are admitted to the clinic the day before or on the day of surgery and undergo general anesthesia. Postoperative hospital stays are 1-3 days for patients undergoing breast reconstruction using breast implants, 3-4 days for patients undergoing TRAM flap reconstruction, and approximately 7-15 days for patients undergoing DIEP flap reconstruction. Apart from routine perioperative procedures, no special procedures are performed for breast reconstruction surgery at the clinic. Patients return to the outpatient clinic for follow-up visits 1-2 weeks after discharge and at one month. At three months postoperatively, the non-reconstructed breast is evaluated for equality with the reconstructed breast, and decisions are made about additional interventions. For patients undergoing core tissue breast reconstruction, the nipple and areola are also reconstructed during this process.
  3. Research Universe and Sample Selection The research universe consisted of patients who underwent breast reconstruction due to breast cancer at GUSAUM Plastic, Reconstructive, and Hand Surgery and Ankara Etlik City Hospital Plastic Surgery Clinic. Inclusion criteria for the study were:
  • Patients who had undergone breast reconstruction surgery due to breast cancer,
  • Patients aged 18 and over,
  • Patients who understood and spoke Turkish,
  • Patients who agreed to participate voluntarily,
  • Patients who were literate. Exclusion criteria included:
  • Patients with speech, hearing, or visual impairments,
  • Patients with a psychiatric diagnosis or ongoing treatment,
  • Patients with metastatic breast cancer,
  • Patients with a cancer diagnosis other than breast cancer. The study termination criteria were:
  • Patients who wished to withdraw from the study during the follow-up period,
  • Patients who had a new cancer history during the follow-up period,
  • Patients who could not be reached when contacted five times in a row during the same week during the follow-up period,
  • Patients who did not regularly participate in the nurse-led coaching program (failing to attend three consecutive sessions or at least five total sessions),
  • Patients who died during the follow-up period.Implementation As a result of the power analysis conducted with the GPower 3.1.9.7 program, to determine the difference in self-care agency measurements between the groups, a sample size of 7 people was determined in each group, for a total of 14 people, based on Type 1 error: 0.05, Type 2 error: 0.20, and Effect Size = 1.636. However, due to differences in the structure of the study and the relatively low sample size, it was not deemed appropriate to use it as a reference. Taking into account the effect size ranges suggested by the program for cases where no similar studies exist, a sample size of 26 people was determined in each group, for a total of 52 people, based on Type 1 error: 0.05, Type 2 error: 0.20, and Effect Size = 0.80, to determine the difference in self-care agency and quality of life measurements between the groups. Taking into account the situation calculated due to possible losses in the study, the sample size was increased by 15%, and it was planned to include 60 people, 30 in each group.
  1. Randomization and Blinding Simple randomization was used in the study. A random number table was used to randomly assign patients to the intervention and control groups. Because the patients in the intervention group were included in the coaching program, blinding of the patients in the study was not possible. Because the nurse-led coaching program was implemented by the researcher, researcher blinding was not possible. During the statistical analysis of the data in the study, the experimental and control group data will be masked, and the statistical analyses will be performed by a different expert, ensuring statistician blinding.
  2. Data Collection Tools Data were collected using the Introductory Information Form, the Self-Care Agency Scale, and the EORTC QLQ-C30 and QLQ-BR42 Quality of Life Scales. 5.1. Introductory Information Form The Introductory Information Form was developed by the researcher based on literature. This form contains a total of 24 questions regarding the individuals' sociodemographic characteristics (age, gender, height, weight, body mass index, marital status, cohabitants, education level, employment status, economic status, family history of breast cancer) and health status. 5.2. Self-Care Agency Scale The Self-Care Agency Scale is a five-point Likert-type scale developed after the concept of self-care was introduced. The scale was developed by Kearney and Fleischer in 1979, and the first version consisted of 43 items. The Turkish version, whose validity and reliability study was conducted by Nahcivan in 1993, was revised to 35 items. Each statement on the scale is scored 0, 1, 2, 3, and 4, respectively. "Describes me a lot" receives 4 points, "Describes me a lot" receives 3 points, "I have no idea" receives 2 points, "Does not describe me" receives 1 point, and "Does not describe me at all" receives 0 points. Eight of the statements (3, 6, 9, 13, 19, 22, 26, and 31) are evaluated negatively, and the scoring is reversed. The highest score that can be obtained from the scale is 140, which represents the highest degree of self-care agency. In the Nahcivan study, Cronbach's alpha value was determined as 0.89. 5.3. EORTC QLQ-C30 and QLQ-BR-42 Quality of Life Scales Developed by the European Organization for Research and Treatment of Cancer, EORTC, the EORTC QLQ-C30 Version 3.0 quality of life scale is a frequently used scale for cancer patients worldwide. The scale consists of 30 questions and three sub-items: general well-being, functional domain (physical function, role function, emotional function, cognitive function, social function), and symptoms (fatigue, nausea and vomiting, pain, shortness of breath, insomnia, loss of appetite, diarrhea, constipation, financial difficulties). The lowest possible score is 0, while the highest is 100. Questions 1-28 are on a four-point Likert-type scale, and questions 29 and 30 are on a seven-point Likert-type scale. Low scores on general well-being and functional domains indicate a decreased quality of life, while high scores indicate a higher quality of life. In the symptoms section, low scores indicate high quality of life, while high scores indicate low quality of life. The Turkish validity and reliability study of the scale was conducted by Beşer and Öz in 2003, and the Cronbach's alpha coefficient was found to be 0.82. The QLQ-BR42 is a continuation of the scale and consists of 42 questions investigating the side effects of breast cancer treatments, body image, sexuality, and future expectations. The scale's scoring is similar to the EORTC QLQ-C30 Version 3.0. Questions related to sexuality are reverse-scored. A high score on the functional domain and a low score on the symptoms section indicate a high quality of life. The validity and reliability study of the scale was conducted by Demirci and colleagues in 2011. 5.4. Program Satisfaction Form This form was administered only to patients who participated in the coaching program in the intervention group and consists of three questions. The questions include three statements measuring the level of self-care ability and quality of life improvement and satisfaction level in relation to the program's goals, and patients are expected to rate them on a scale of 1-10 (1-none, 10-very).
  3. Application of the Research 6.1. Researcher Preparation To learn the art and competencies specific to the coaching profession, the researcher received two modules of training: 64 hours of theory and 16 hours of practical training from Anka Coaching, an institution accredited by the International Coach Federation (ICF) and the Association for Coaching (AC). As a result of these trainings, the researcher received the Art and Competencies of Coaching Certificate and the Holistic Life Coaching Certificate. At the end of the training, the researcher recorded one of her coaching sessions, which were listened to and evaluated by ICF mentors and deemed appropriate. As a result of this evaluation, the researcher was awarded the Holistic Coaching Certificate. The researcher developed her coaching skills by conducting voluntary coaching sessions. During the pre-implementation phase, the researcher conducted a total of six coaching sessions with two patients to gain experience in conducting coaching sessions with patients undergoing breast reconstruction surgery and to evaluate the effectiveness of the coaching program. 6.2 Nurse-Led Coaching Program for Breast Reconstruction Patients The Nurse-Led Coaching Program for Breast Reconstruction Patients was developed by a researcher. The program includes literature review, the program's purpose, objectives, target audience, program flow, forms to be used in all coaching sessions, and coaching tools to be used when needed. Expert opinions were obtained from a total of nine experts regarding the Nurse-Led Coaching Program for Breast Reconstruction Patients. Three of the experts are MCC (Master Certified Coach - the highest-level title awarded to coaches) and are qualified in the field of coaching. The other experts are nursing academics who have also received coaching training and certification. A form was sent to the experts to provide their recommendations for all steps. The experts evaluated all sections of the program using a four-point Likert-type scale (1: not appropriate, 2: somewhat appropriate - major change needed, 3: appropriate - minor change needed, 4: very appropriate) and provided their recommendations on the prepared form. Based on expert opinions, the program's content validity ratio (CVR) was calculated using the Lawshe technique. The minimum value was determined as 0.75 based on the minimum values table for content validity ratios at a significance level of α=0.05 developed by Veneziano and Hooper. Analyses indicated that some sections of the program needed modifications. The coaching program was updated and revised based on feedback from the experts. The program's functionality was evaluated through a pre-implementation. As part of the Nurse-Led Coaching Program for Breast Reconstruction Patients, patients received coaching sessions for 12 weeks after discharge. There are differing opinions in the literature regarding the frequency and duration of coaching sessions. However, professional coaches trained by the International Coach Federation (ICF) and Association for Coaching (AC) recommend the frequency and duration of coaching sessions for each designated topic, three or four times a month, lasting approximately 35 minutes. Accordingly, a total of nine coaching sessions were conducted with the patients in the intervention group: weekly for the first 6 weeks after discharge and biweekly for the following 6 weeks. Each coaching session lasted an average of 30-40 minutes. Coaching sessions were conducted via online video calls using applications such as Zoom, WhatsApp, Skype, and Google Meets, as appropriate for the patient. In the first week, the nature of coaching was discussed with the patient, a coaching agreement was signed, and forms to assist with goal planning and agenda setting were introduced. In the second week, a Values Study for Breast Reconstruction Patients was conducted with the patient. In the third week, the Wheel of Life for Breast Reconstruction Patients was implemented, and in the fourth week, a SWOT Analysis for Breast Reconstruction Patients was conducted. In the following weeks, coaching sessions were conducted based on the agenda set by the patient. At the end of the coaching sessions, the patients were assessed for achievement of the goals they had set at the beginning of the session. A final counseling session was held 12 weeks after discharge, and the Wheel of Life was implemented again. The overall process and the effectiveness of the program were evaluated with the patient.
  4. Data Evaluation The Statistical Package for Social Science (SPSS) 25.0 will be used for statistical analysis of the research data. Numbers, percentages, mean, and standard deviation values will be used to evaluate descriptive data. The Shapiro-Wilk test will assess compliance with a normal distribution. A t-test and a One-Way Analysis of Variance (ANOVA) for Repeated Measures will be used to compare the pretest and posttest mean scores of the intervention and control groups. A p value of <0.05 will be considered statistically significant. Intention-to-treat (ITT) analysis will be used for losses in the sample group during follow-up.
  5. Ethical Aspects of the Research Permission for the study was obtained from the Gazi University Ethics Committee and the institutions where the study would be conducted. Written informed consent forms were signed by the patients participating in the study. Furthermore, the necessary permissions for the use of the data collection forms were obtained. After the study is concluded, patients in the control group will be contacted and voluntary coaching sessions (minimum 4 sessions) will be held for those who request it.
Being tested
Nurse-led Coaching Program
Keywords
nursing, coaching, quality of life, self-care agency, Breast Reconstruction

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Nurse-led Coaching ProgramBehavioural

    This intervention is implemented to increase patients' quality of life and self-care agency.

Study groups in NCT07355946
Study groupRoleWhat they receive
Control GroupNo interventionNot described
Intervention GroupExperimentalA total of 9 sessions of nurse-led coaching program are implemented for the intervention group over 12 weeks.
Receives: Behavioral: Nurse-led Coaching Program

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Self-care Agency Scale

    The Self-Care Agency Scale is a five-point Likert-type scale developed after the concept of self-care was introduced. The scale was developed by Kearney and Fleischer in 1979, and the first version consisted of 43 items (Kearney \& Fleischer, 1979). The Turkish version, whose validity and reliability study was conducted by Nahcivan in 1993, was revised to 35 items. Each statement on the scale is scored 0, 1, 2, 3, and 4, respectively. "Describes me very much" receives 4 points, "Describes me very much" receives 3 points, "I have no idea" receives 2 points, "Does not describe me at all" receives 1 point, and "Does not describe me at all" receives 0 points. Eight of the statements (3, 6, 9, 13, 19, 22, 26, and 31) are evaluated negatively, and the scoring is reversed. The highest possible score on the scale is 140, representing the highest degree of self-care agency. In the Nahcivan study, Cronbach's alpha was determined to be 0.89.

    Measured: From enrollment to the end of coaching program at 12 weeks

Secondary outcomes (1)
  1. EORTC QLQ-C30 Quality of Life Scale

    Developed by the European Organization for Research and Treatment of Cancer (EORTC) (2001), the EORTC QLQ-C30 Version 3.0 Quality of Life Scale is a frequently used measure for cancer patients worldwide. The scale consists of 30 questions and three sub-items: general well-being, functional domain and symptoms.

    Measured: From enrollment to the end of coaching program at 12 weeks

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted21 Jan 2026
  2. Study start24 Feb 2025
  3. Primary completion1 Dec 2025
  4. Study completion1 Dec 2025

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Supportive care
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
58 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07355946
Sponsor's protocol ID
E-77082166-302.08.01-1195604
Status last verified
May 2026
First submitted
28 Dec 2025
Last updated
28 May 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: Data supporting this study are not publicly available due to ethical reasons but the datasets used and/or analyzed during the current study are available by emailing sevil.guler@gazi.edu.tr and nihalyildizemre@kku.edu.tr upon reasonable request.

Questions about this trial

What is this clinical trial studying?

A study testing Nurse-led Coaching Program in people with Breast Reconstruction, run by Gazi University at 1 site in Turkey (Türkiye).

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 5 inclusion and 4 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 28 May 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Turkey (Türkiye). Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Self-care Agency Scale (time frame: From enrollment to the end of coaching program at 12 weeks). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 28 May 2026.

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