A Guided Internet-delivered Individually-tailored ACT-influenced CBT Intervention to Improve Psychosocial Outcomes in Breast Cancer (INNOVBC)
Primary Purpose
Breast Neoplasm
Status
Unknown status
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
iACT-BC
Sponsored by
About this trial
This is an interventional supportive care trial for Breast Neoplasm focused on measuring Breast Cancer, Survivors, Internet intervention, Psychosocial intervention, Acceptance and Commitment Therapy (ACT), Randomized controlled trial
Eligibility Criteria
Inclusion Criteria:
- Signed written informed consent.
- Age ≥ 18 years;
- Ability to read and write in Portuguese.
- History of histologically or cytologically confirmed breast cancer with no evidence of metastatic disease.
- An interval ≥ 6 month from primary adjuvant treatment completion (surgery, chemotherapy and/or radiotherapy), except for hormonal therapy.
- Clinically significant symptoms of at least one of the following conditions: anxiety, depression, fatigue, insomnia and/or sexual dysfunction.
- Ongoing regular psychoactive medication only accepted if dosage has been stable during the last 3 months.
- Daily access to the Internet by computer and/or smartphone.
- Ability to use a computer and/or smartphone and the internet.
- No participation on any other interventional study or clinical trial.
Exclusion Criteria:
- Age ≤ 18 years;
- Inability to co-operate and give informed consent.
- Breast cancer not histologically or cytologically confirmed.
- History of other malignancy within the last 5 years.
- Metastasized breast cancer.
- Current severe, uncontrolled systemic disease or mental disorder.
- Absence of clinically significant symptoms.
- Parallel ongoing psychological treatment.
- Ongoing regular psychoactive medication if dosage has been changed during the last 3 months.
- No access to the internet.
- Inability to use a computer and/or smartphone and the internet.
- Parallel ongoing participation in other interventional study or clinical trial.
- Assessment by the investigator to be unable or unwilling to comply with the requirements of the protocol.
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Other
Arm Label
A - iACT-BC experimental group
B - Waiting list control group
Arm Description
Outcomes
Primary Outcome Measures
Depression
Patient Health Questionnaire (PHQ-9)
Anxiety
Generalized Anxiety Disorder Scale (GAD-7)
Secondary Outcome Measures
Psychological flexibility
Cancer Acceptance and Action Questionnaire (Cancer AAQ)
Fatigue
Brief Fatigue Inventory (BFI)
Insomnia
Insomnia Severity Index (ISI)
Sexual dysfunction
Female Sexual Function Index (FSFI)
Health related quality of life - generic measure
EORTC QLQC30
Health related quality of life - breast cancer specific measure
EORTC QLQBR23
Full Information
NCT ID
NCT03275727
First Posted
September 1, 2017
Last Updated
September 7, 2017
Sponsor
Linkoeping University
Collaborators
Universidade Nova de Lisboa
1. Study Identification
Unique Protocol Identification Number
NCT03275727
Brief Title
A Guided Internet-delivered Individually-tailored ACT-influenced CBT Intervention to Improve Psychosocial Outcomes in Breast Cancer
Acronym
INNOVBC
Official Title
Self-care Programs in Oncology: a Guided Internet-delivered Individually-tailored Acceptance and Commitment Therapy (ACT)-Influenced Cognitive Behavioural Intervention to Improve Psychosocial Outcomes in Breast Cancer Survivors
Study Type
Interventional
2. Study Status
Record Verification Date
September 2017
Overall Recruitment Status
Unknown status
Study Start Date
February 2018 (Anticipated)
Primary Completion Date
December 2019 (Anticipated)
Study Completion Date
December 2019 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Linkoeping University
Collaborators
Universidade Nova de Lisboa
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
5. Study Description
Brief Summary
Background: Internet-delivered interventions (IDI) can provide remarkable opportunities in addressing breast cancer (BC) survivors' unmet needs, as they present an effective strategy to improve care coordination and provide access to efficacious, cost-efficient and convenient survivorship care. Nevertheless, research focusing on this field and aiming at improving survivors´ psychosocial needs is scarce and its practical implementation is limited.
Objectives: This study aims at studying BC patients´ and healthcare providers' attitudes towards IDI; exploring BC patients´ unmet support needs and; determining the acceptability, feasibility, efficacy and cost-effectiveness of iACT-BC, a guided internet-delivered individually-tailored ACT-influenced cognitive behavioural intervention designed to improve psychosocial outcomes in BC survivors when compared to treatment as usual. The primary outcomes in this research are anxiety and depression. Secondary outcomes include psychological flexibility, fatigue, insomnia, Sexual dysfunction (SD) and Health Related Quality of Life.
Methods: A multimethod research design will be applied and two consecutive studies will be performed. Study 1 will explore participants´ attitudes towards IDI as well as, BC patients' psychosocial unmet needs by adopting an exploratory cross-sectional study design. Study 2 will investigate the effectiveness and cost-effectiveness of iACT-BC in BC survivors, by implementing a two-arm, parallel, open label, multicentre, waiting list randomized controlled trial.
Expected Results: It is anticipated that iACT-BC will show to be an effective and cost-effective program in improving anxiety, depression, psychological flexibility, fatigue, insomnia, SD and HRQoL in BC survivors, as opposing to a waiting list control under treatment as usual. The results of this research will be published in accordance with CONSORT 2010 and CONSORT-EHEALTH guidelines and should be available for publication in February 2020.
Detailed Description
Background: Breast Cancer (BC) ranks as the most frequent and lethal cancer among women, in Portugal. However, advances in cancer detection and treatment contributed to a steady and significant increase in survival over the past years, and 5-year age-standardized relative survival is currently estimated to be 83,4%. This increase translates into a high and growing number of BC survivors, with a considerable proportion of these patients experiencing sequelae of treatment and late effects that can occur immediately to several years after primary treatment ends. Anxiety, depression, fear of recurrence, existential related issues, fatigue, pain, physical and cognitive impairment, tailored information needs, and sexual dysfunction have been reported as the most common unmet support care needs experienced by these women. The answer to these unmet support care needs relies, in part, on delivering comprehensive, highly coordinated, patient-centred care. However, operationalizing such care may prove difficult in a context of competing priorities and constrained health and social care budgets. In this context, connected health, particularly internet-delivered interventions, can provide remarkable opportunities in overcoming the aforementioned constraints, as presenting an effective and innovative healthcare delivery model capable of improving care coordination and providing access to efficacious, cost-efficient and convenient survivorship care. Nevertheless, research focusing on this field and aiming at improving survivors´ psychosocial needs is scarce and its practical implementation is limited.
Objectives: The objectives of this investigation are: studying BC patients´ and healthcare providers' attitudes towards internet-delivered interventions; exploring breast cancer patients´ unmet support care needs and; determining the acceptability, feasibility, effectiveness and cost-effectiveness of iACT-BC, a guided internet-delivered individually-tailored Acceptance and Commitment Therapy (ACT)-influenced cognitive behavioural intervention designed to improve psychosocial outcomes in BC survivors when compared to treatment as usual (TAU) in a waiting list control group (WLC). The primary outcomes in this research are anxiety and depression. Secondary outcomes include psychological flexibility, fatigue, insomnia, sexual dysfunction and Health Related Quality of Life (HRQoL).
Hypotheses: We hypothesize that participants in the intervention group will have improved anxiety, depression, psychological flexibility, fatigue, insomnia, sexual dysfunction and HRQoL, when compared to a WLC.
Methods: A multimethod research design will be applied and two consecutive studies will be performed: Study 1 - Population characterization study and Study 2 - Efficacy and cost-effectiveness study. Study 1 will explore participants´ attitudes towards internet-delivered interventions as well as, BC patients' psychosocial unmet support needs by adopting an exploratory cross-sectional study design. Study 2 will investigate the effectiveness and cost-effectiveness of iACT-BC in BC survivors, by implementing a two-arm, parallel, open label, multicentre, pragmatic, waiting list randomized controlled trial. A Pilot study, mirroring the conditions applied in Study 2 should be performed in order to evaluate the feasibility and acceptability of iACT-BC. Results from this Pilot study should be appraised and inform execution of Study 2
Ethical approval: This study will soon be submitted to evaluation by CNPD and local ethic committees. Authorization to run the study is expected to be received until January 2018.
Expected Results: It is anticipated that iACT-BC will show to be an effective and cost-effective program in improving psychosocial outcomes such as anxiety, depression, psychological flexibility, fatigue, insomnia, sexual dysfunction and HRQoL in BC survivors, as opposing to a WLC under TAU. The results of this research will be published in accordance with CONSORT 2010 and CONSORT-EHEALTH guidelines and should be available for publication in February 2020.
Keywords: Breast Cancer; Survivors; Internet intervention; Psychosocial intervention; Acceptance and Commitment Therapy (ACT); Randomized controlled trial protocol.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Neoplasm
Keywords
Breast Cancer, Survivors, Internet intervention, Psychosocial intervention, Acceptance and Commitment Therapy (ACT), Randomized controlled trial
7. Study Design
Primary Purpose
Supportive Care
Study Phase
Phase 2, Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
128 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
A - iACT-BC experimental group
Arm Type
Experimental
Arm Title
B - Waiting list control group
Arm Type
Other
Intervention Type
Behavioral
Intervention Name(s)
iACT-BC
Intervention Description
A Guided INternet-delivered Individually-tailored ACT-influenced Cognitive Behavioural INtervention to ImprOVe Psychosocial Outcomes in Breast Cancer Survivors
Primary Outcome Measure Information:
Title
Depression
Description
Patient Health Questionnaire (PHQ-9)
Time Frame
Change from baseline to post-intervention (10 weeks after enrollment), Follow-ups at 3, 6 and 12 months
Title
Anxiety
Description
Generalized Anxiety Disorder Scale (GAD-7)
Time Frame
Change from baseline to post-intervention (10 weeks after enrollment), Follow-ups at 3, 6 and 12 months
Secondary Outcome Measure Information:
Title
Psychological flexibility
Description
Cancer Acceptance and Action Questionnaire (Cancer AAQ)
Time Frame
Change from baseline to post-intervention (10 weeks after enrollment), Follow-ups at 3, 6 and 12 months
Title
Fatigue
Description
Brief Fatigue Inventory (BFI)
Time Frame
Change from baseline to post-intervention (10 weeks after enrollment), Follow-ups at 3, 6 and 12 months
Title
Insomnia
Description
Insomnia Severity Index (ISI)
Time Frame
Change from baseline to post-intervention (10 weeks after enrollment), Follow-ups at 3, 6 and 12 months
Title
Sexual dysfunction
Description
Female Sexual Function Index (FSFI)
Time Frame
Change from baseline to post-intervention (10 weeks after enrollment), Follow-ups at 3, 6 and 12 months
Title
Health related quality of life - generic measure
Description
EORTC QLQC30
Time Frame
Change from baseline to post-intervention (10 weeks after enrollment), Follow-ups at 3, 6 and 12 months
Title
Health related quality of life - breast cancer specific measure
Description
EORTC QLQBR23
Time Frame
Change from baseline to post-intervention (10 weeks after enrollment), Follow-ups at 3, 6 and 12 months
Other Pre-specified Outcome Measures:
Title
Participants' attitudes towards internet interventions
Description
Attitudes towards internet interventions survey (ATTIS)
Time Frame
Change from baseline to post-intervention (10 weeks after enrollment), Follow-ups at 3, 6 and 12 months
Title
Breast cancer patients' unmet support needs
Description
Supportive Care Needs Survey Questionnaire (SCNS-SF34)
Time Frame
Change from baseline to post-intervention (10 weeks after enrollment), Follow-ups at 3, 6 and 12 months
Title
Intervention cost-effectiveness
Description
Questionnaire on Medical consumption and Productivity losses associated with Psychiatric Illness (TIC-P)
Time Frame
Change from baseline to post-intervention (10 weeks after enrollment), Follow-ups at 3, 6 and 12 months
Title
Intervention cost-utility
Description
EuroQol EQ-5D-5L
Time Frame
Change from baseline to post-intervention (10 weeks after enrollment), Follow-ups at 3, 6 and 12 months
10. Eligibility
Sex
Female
Gender Based
Yes
Gender Eligibility Description
Only female BC survivors
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Signed written informed consent.
Age ≥ 18 years;
Ability to read and write in Portuguese.
History of histologically or cytologically confirmed breast cancer with no evidence of metastatic disease.
An interval ≥ 6 month from primary adjuvant treatment completion (surgery, chemotherapy and/or radiotherapy), except for hormonal therapy.
Clinically significant symptoms of at least one of the following conditions: anxiety, depression, fatigue, insomnia and/or sexual dysfunction.
Ongoing regular psychoactive medication only accepted if dosage has been stable during the last 3 months.
Daily access to the Internet by computer and/or smartphone.
Ability to use a computer and/or smartphone and the internet.
No participation on any other interventional study or clinical trial.
Exclusion Criteria:
Age ≤ 18 years;
Inability to co-operate and give informed consent.
Breast cancer not histologically or cytologically confirmed.
History of other malignancy within the last 5 years.
Metastasized breast cancer.
Current severe, uncontrolled systemic disease or mental disorder.
Absence of clinically significant symptoms.
Parallel ongoing psychological treatment.
Ongoing regular psychoactive medication if dosage has been changed during the last 3 months.
No access to the internet.
Inability to use a computer and/or smartphone and the internet.
Parallel ongoing participation in other interventional study or clinical trial.
Assessment by the investigator to be unable or unwilling to comply with the requirements of the protocol.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Cristina M Santos, MsC
Phone
+351917890798
Email
cristina.mendes.santos@liu.se
First Name & Middle Initial & Last Name or Official Title & Degree
Gerhard Andersson, PhD
Email
gerhard.andersson@liu.se
12. IPD Sharing Statement
Plan to Share IPD
No
Citations:
PubMed Identifier
30949435
Citation
Mendes-Santos C, Weiderpass E, Santana R, Andersson G. A guided internet-delivered individually-tailored ACT-influenced cognitive behavioural intervention to improve psychosocial outcomes in breast cancer survivors (iNNOVBC): Study protocol. Internet Interv. 2019 Feb 10;17:100236. doi: 10.1016/j.invent.2019.01.004. eCollection 2019 Sep.
Results Reference
derived
Links:
URL
https://innovbc.iterapi.se
Description
Study website
Learn more about this trial
A Guided Internet-delivered Individually-tailored ACT-influenced CBT Intervention to Improve Psychosocial Outcomes in Breast Cancer
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