search
Back to results

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
Linkoeping University
About
Eligibility
Locations
Arms
Outcomes
Full info

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

18 Years - undefined (Adult, Older Adult)FemaleDoes not accept healthy volunteers

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

    First Posted
    September 1, 2017
    Last Updated
    September 7, 2017
    Sponsor
    Linkoeping University
    Collaborators
    Universidade Nova de Lisboa
    search

    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

    We'll reach out to this number within 24 hrs