Effects of a Lay-led Anxiety and Depression Self-management Program for Cancer Patients (ADSMP-C)
Primary Purpose
Neoplasms, Anxiety, Self Efficacy
Status
Recruiting
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
ADSMP-C
Sponsored by
About this trial
This is an interventional treatment trial for Neoplasms focused on measuring Intervention, RCT
Eligibility Criteria
Inclusion Criteria:
- Treated in Central Region Denmark
- Recently completed (< 1 yr.) primary treatment for cancer with curative intent
- BDI-II score >=14 and/or STAI-state score >=40
Exclusion Criteria:
- Not sufficient Danish language skills to fill Questionnaires and participate in a group based intervention
- Psychosis
- Aggressive behavior
- Imminent suicidal risk
Sites / Locations
- Dep. Oncology, Aarhus University HospitalRecruiting
- Dep. Oncology, Regional Hospital West JutlandRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
No Intervention
Arm Label
Intervention Group
Control Group
Arm Description
ADSMP-C
Wait-list control group
Outcomes
Primary Outcome Measures
Change in Depressive Symptoms
Beck Depression Inventory (BDI-II)
Change in Anxiety Symptoms
Spielberger State-Trait Inventory (STAI). State subscale.
Secondary Outcome Measures
Change in Anxiety Symptoms
Spielberger State-Trait Inventory (STAI). State subscale.
Change in Depressive Symptoms
Beck Depression Inventory (BDI-II)
Change in Anxiety (observer-rated)
Hamilton Anxiety Rating Scale (HAM-A6)
Change in Depression (observer-rated)
Hamilton Depression Rating Scale (HAM-D6)
Change in Fear of cancer recurrence
Concerns About Recurrence Questionaire (CARQ-4)
Change in Self-efficacy - Personal control
The Revised Illness Perception Questionnaire (IPQ-R). Personal Control subscale.
Change in Self-efficacy - Social support
Obtain Help from Community, Family, Friends Scale (SECD-Ssup)
Full Information
NCT ID
NCT04537195
First Posted
August 27, 2020
Last Updated
May 10, 2023
Sponsor
University of Aarhus
Collaborators
TrygFonden, Denmark, Komiteen for Sundhedsoplysning, Aarhus University Hospital
1. Study Identification
Unique Protocol Identification Number
NCT04537195
Brief Title
Effects of a Lay-led Anxiety and Depression Self-management Program for Cancer Patients
Acronym
ADSMP-C
Official Title
Effects on Anxiety and Depression of a Lay-led Transdiagnostic Self-management Program (ADSMP-C) for Patients Recently Treated for Cancer With Curative Intent: A Randomized Controlled Trial
Study Type
Interventional
2. Study Status
Record Verification Date
May 2023
Overall Recruitment Status
Recruiting
Study Start Date
March 6, 2020 (Actual)
Primary Completion Date
October 31, 2023 (Anticipated)
Study Completion Date
April 1, 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of Aarhus
Collaborators
TrygFonden, Denmark, Komiteen for Sundhedsoplysning, Aarhus University Hospital
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
The investigators aim to evaluate a peer-to-peer patient self-management program targeting symptoms of anxiety and depression in a randomized trial. A total of 234 cancer patients recently having completed primary treatment with curative intent in central Region Denmark will be included. The intervention is a lay-led, group-based transdiagnostic patient education program consisting of seven 2 ½ hour weekly sessions focusing on increasing patient self-efficacy in symptom management of anxiety and depression. The intervention is highly structured and manualized.
Detailed Description
Recent evidence suggest that transdiagnostic interventions may be just as effective as traditional diagnosis specific interventions when treating symptoms of depression and anxiety. Brief lay-led transdiagnostic self-management interventions may therefore offer an efficient alternative to traditional symptom specific interventions (e.g. CBT) when targeting symptoms of depression and anxiety in cancer.
The present study aim to evaluate The Anxiety and Depression Symptom Management Program (ADSMP) in a cancer setting (ADSMP-C). The ADSMP is a Danish adaptation of The Stanford University Chronic Disease Self-Management Program (CDSMP) and is developed by the Danish Health Information Committee (In Danish: Komiteen for Sundhedsoplysning in collaboration with The Expert Patient Program Community Interest Company (EPPCIC), the English Health Service (NHS) and Stanford University.
The ADSMP-C is a lay-led, group-based transdiagnostic patient education program consisting of seven 2 ½ hour weekly sessions focusing on increasing patient self-efficacy in symptom management of anxiety and depression concluded with a networking session. The intervention is highly structured and manualized. Sub-group analyses on participants with a history of cancer in a larger trial of ADSMP conducted by members of the study group on behalf of the Danish National Board of Health showed promising results. However, a larger study is needed to establish sound scientific evidence on the effectiveness of the program in a cancer setting.
A total 234 cancer patients recently having completed primary treatment with curative intent in central Region Denmark will be randomized (2:1) to ADSMP-C or a control arm respectively. As a part of the recruitment procedure patients will be screened with The "Distress-Thermometer" at the departments of oncology at the two largest hospitals in Central Region, Denmark following primary treatment or at a follow-up (< 1yrs. after primary treatment).
Participants completes online questionnaires (REDCap) at baseline (pre-randomization), at post-intervention, and at three (primary follow-up) and six months post-intervention, including the Beck's Depression Inventory (BDI-II) and Spielbergers State-Trait Anxiety Inventory (STAI-state) (primary outcomes). In addition, all participants will be interviewed at 7 month post-intervention. Outcome assessors, blind to group allocation, will perform observer-based Hamilton A6 and D6 short-form ratings at the interview (secondary outcomes).
Data will be evaluated by mixed-effects regression analyses (intention-to-treat).
The current study will be the first to evaluate the efficacy of ADSMP in a cancer setting.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Neoplasms, Anxiety, Self Efficacy, Psychological Distress, Cancer, Distress, Emotional, Depression, Group, Peer
Keywords
Intervention, RCT
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Masking Description
Assessors will be blinded at 7-month follow-up when administering the Hamilton rating scales (secondary outcomes). Participants will be instructed not to disclose their group allocation until the interview is completed
Allocation
Randomized
Enrollment
234 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Intervention Group
Arm Type
Experimental
Arm Description
ADSMP-C
Arm Title
Control Group
Arm Type
No Intervention
Arm Description
Wait-list control group
Intervention Type
Behavioral
Intervention Name(s)
ADSMP-C
Intervention Description
A transdiagnostic, lay-led, group-based self-management program consisting of seven 2 ½ hour weekly sessions focusing on increasing patient self-efficacy in symptom management of anxiety and depression in cancer (ADSMP-C)
Primary Outcome Measure Information:
Title
Change in Depressive Symptoms
Description
Beck Depression Inventory (BDI-II)
Time Frame
Baseline and 3 months post-intervention
Title
Change in Anxiety Symptoms
Description
Spielberger State-Trait Inventory (STAI). State subscale.
Time Frame
Baseline and 3 months post-intervention
Secondary Outcome Measure Information:
Title
Change in Anxiety Symptoms
Description
Spielberger State-Trait Inventory (STAI). State subscale.
Time Frame
Baseline and 6 months post-intervention
Title
Change in Depressive Symptoms
Description
Beck Depression Inventory (BDI-II)
Time Frame
Baseline and 6 months post-intervention
Title
Change in Anxiety (observer-rated)
Description
Hamilton Anxiety Rating Scale (HAM-A6)
Time Frame
Baseline and 7 months post-intervention
Title
Change in Depression (observer-rated)
Description
Hamilton Depression Rating Scale (HAM-D6)
Time Frame
Baseline and 7 months post-intervention
Title
Change in Fear of cancer recurrence
Description
Concerns About Recurrence Questionaire (CARQ-4)
Time Frame
Baseline and 3 months post-intervention
Title
Change in Self-efficacy - Personal control
Description
The Revised Illness Perception Questionnaire (IPQ-R). Personal Control subscale.
Time Frame
Baseline and 3 months post-intervention
Title
Change in Self-efficacy - Social support
Description
Obtain Help from Community, Family, Friends Scale (SECD-Ssup)
Time Frame
Baseline, and 3 months post-intervention
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Treated in Central Region Denmark
Recently completed (< 1 yr.) primary treatment for cancer with curative intent
BDI-II score >=14 and/or STAI-state score >=40
Exclusion Criteria:
Not sufficient Danish language skills to fill Questionnaires and participate in a group based intervention
Psychosis
Aggressive behavior
Imminent suicidal risk
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Soren Christensen, MSc.
Phone
(+45) 8716 5876
Email
sc@psy.au.dk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Soren Christensen, MSc.
Organizational Affiliation
Dep. Psychology, Aarhus University, Denmark
Official's Role
Principal Investigator
Facility Information:
Facility Name
Dep. Oncology, Aarhus University Hospital
City
Aarhus
ZIP/Postal Code
8000
Country
Denmark
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Anders B Jensen, MD, PhD
Email
Anders.Bonde.Jensen@auh.rm.dk
First Name & Middle Initial & Last Name & Degree
Anders B Jensen, MD, PhD
Facility Name
Dep. Oncology, Regional Hospital West Jutland
City
Herning
ZIP/Postal Code
7400
Country
Denmark
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Halla O Skuladottir, PhD, DMSc
Phone
(+45) 78437400
Email
hallskul@rm.dk
First Name & Middle Initial & Last Name & Degree
Halla O Skuladottir, PhD, DMSc
12. IPD Sharing Statement
Plan to Share IPD
No
IPD Sharing Plan Description
At the present the policy of Aarhus University does not allow the sharing of data according to GDPR rules. However this policy may be subject to change
Learn more about this trial
Effects of a Lay-led Anxiety and Depression Self-management Program for Cancer Patients
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