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Stress Management Intervention in Early Stage Cancer: Randomized Controlled Trial

Primary Purpose

Cancer, Stress, Psychological

Status
Active
Phase
Not Applicable
Locations
Norway
Study Type
Interventional
Intervention
App for stress management
Sponsored by
Oslo University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Cancer focused on measuring Stress management, App

Eligibility Criteria

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

Inclusion Criteria:

  • Patients diagnosed with cancer (all diagnosis).
  • Maximum time since completed treatment at hospital: 12 months
  • Patients are > 18 years of age, able to write/read/speak Norwegian and have their own smart phone or tablet

Exclusion Criteria:

• None

Sites / Locations

  • Oslo University hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

App for Stress management

Waitlist control group

Arm Description

Participants will get access to two modules per week for five weeks (total 10 modules). The app consists of stress management education, cognitive behavioral interventions and relaxation training exercises.

Participants will get treatment as usual during the study. After the one year study follow up they will receive the stress management app.

Outcomes

Primary Outcome Measures

The Perceived Stress Scale (PSS-14)
14 item scale measuring perceived stress. Scale range: 0-56. Higher scores indicate higher perceived stress.

Secondary Outcome Measures

SF-36 Item Short Form Health Survey (RAND-36 version)
36 item scale measuring health related quality of life (HRQoL). The scale has 8 subscales and 1 single item score. Scale and single item range: 0 to 100. Higher scores indicate higher HRQoL.
The Self-Regulatory Fatigue-18 (SRF-18)
18 item scale measuring self-regulation. Scale range: 18 to 90. A higher score indicates higher self regulatory fatigue
The Brief Coping Orientation to Problems (Brief COPE)
The outcome measure consists of 14 different scales of different coping strategies with two items per scale, for a total of 28 items. Scale range 2 to 8. Higher scores indicate higer use of the different coping strategies
Health, well-being and sleep
A 5 item measure, measuring health, well-being and sleep on a scale from 0 to 10. Higher scores indicate better health, well-being and sleep
Intervention commentary
A six item brief measure of participant's intervention reactions. The first 3 items gauged participants' program perception on a scale from 1 to 5, with 5 indicating better perception. The next 3 items were open ended questions: * What did you like best? * What did you like the least? * Suggestions for improvement?
The Hospital Anxiety and Depression Scale (HADS)
14 item scale measuring anxiety and depression. The Scale has a total score with a scale range of 0 to 42 and an anxiety (HADS-A) and a depression (HADS-D) subscale, both with scale range of 0 to 21. Higer scores indicate higher level of anxiety and depression
The Distress Thermometer
One item scale measuring distress on a scale from 0 to 10. Higer scores indicate higher distress

Full Information

First Posted
October 17, 2016
Last Updated
October 10, 2022
Sponsor
Oslo University Hospital
Collaborators
Norwegian Cancer Society
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1. Study Identification

Unique Protocol Identification Number
NCT02939612
Brief Title
Stress Management Intervention in Early Stage Cancer: Randomized Controlled Trial
Official Title
Testing a Computerized Interactive Stress Management Intervention in Early Stage Cancer: A Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
October 2022
Overall Recruitment Status
Active, not recruiting
Study Start Date
October 2016 (undefined)
Primary Completion Date
August 2020 (Actual)
Study Completion Date
December 31, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Oslo University Hospital
Collaborators
Norwegian Cancer Society

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose with this study is to test the effect of an app for stress management among patients with a variety of cancer diagnoses.
Detailed Description
A cancer diagnosis and subsequent treatment can be disruptive and traumatic, often accompanied by a multitude of stressors for the patients and their support network. Uncertainty of outcome and invasive medical procedures with aversive side effects are not uncommon, and while people differ widely in how they experience and cope with such challenges, cancer related distress including anxiety, depression, worry and rumination is prevalent. With multiple domains of function impacted it is also not surprising that quality of life (QoL) often is diminished. Stress management interventions can facilitate adjustment to cancer, including reduced distress and improved quality of life. Unfortunately, many people with cancer do not have the strength or opportunity to attend groups or in-person interventions. This study will therefore test the effect of an app for stress management among patients with different cancer diagnosis. The app contains 10 modules distributed over five weeks, focusing on education of different techniques for reduction of stress and stress reduction exercises. The app was tested in a feasibility pilot study among 25 patients with a variety of cancer diagnoses and is now being tested in a randomized controlled trial with a sample of 175 cancer survivors. The participants were randomly assigned to use the 10 module app or to a control group that receive treatment as usual, and will be followed with repeated measures over 12 months.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cancer, Stress, Psychological
Keywords
Stress management, App

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
200 (Actual)

8. Arms, Groups, and Interventions

Arm Title
App for Stress management
Arm Type
Experimental
Arm Description
Participants will get access to two modules per week for five weeks (total 10 modules). The app consists of stress management education, cognitive behavioral interventions and relaxation training exercises.
Arm Title
Waitlist control group
Arm Type
No Intervention
Arm Description
Participants will get treatment as usual during the study. After the one year study follow up they will receive the stress management app.
Intervention Type
Behavioral
Intervention Name(s)
App for stress management
Other Intervention Name(s)
Stress management
Intervention Description
An app consisting of 10 modules that teaches stress management, cognitive behavioral coping skills and relaxation training.
Primary Outcome Measure Information:
Title
The Perceived Stress Scale (PSS-14)
Description
14 item scale measuring perceived stress. Scale range: 0-56. Higher scores indicate higher perceived stress.
Time Frame
Baseline, post intervention follow up at 3, 6, and 12 months
Secondary Outcome Measure Information:
Title
SF-36 Item Short Form Health Survey (RAND-36 version)
Description
36 item scale measuring health related quality of life (HRQoL). The scale has 8 subscales and 1 single item score. Scale and single item range: 0 to 100. Higher scores indicate higher HRQoL.
Time Frame
Baseline, post intervention follow up at 3, 6, and 12 months
Title
The Self-Regulatory Fatigue-18 (SRF-18)
Description
18 item scale measuring self-regulation. Scale range: 18 to 90. A higher score indicates higher self regulatory fatigue
Time Frame
Baseline, post intervention follow up at 3 and 12 months
Title
The Brief Coping Orientation to Problems (Brief COPE)
Description
The outcome measure consists of 14 different scales of different coping strategies with two items per scale, for a total of 28 items. Scale range 2 to 8. Higher scores indicate higer use of the different coping strategies
Time Frame
Baseline
Title
Health, well-being and sleep
Description
A 5 item measure, measuring health, well-being and sleep on a scale from 0 to 10. Higher scores indicate better health, well-being and sleep
Time Frame
Baseline, post intervention follow up at 3, 6, and 12 months
Title
Intervention commentary
Description
A six item brief measure of participant's intervention reactions. The first 3 items gauged participants' program perception on a scale from 1 to 5, with 5 indicating better perception. The next 3 items were open ended questions: * What did you like best? * What did you like the least? * Suggestions for improvement?
Time Frame
Post intervention (immediately post intervention)
Title
The Hospital Anxiety and Depression Scale (HADS)
Description
14 item scale measuring anxiety and depression. The Scale has a total score with a scale range of 0 to 42 and an anxiety (HADS-A) and a depression (HADS-D) subscale, both with scale range of 0 to 21. Higer scores indicate higher level of anxiety and depression
Time Frame
Baseline, post intervention follow up at 3, 6, and 12 months
Title
The Distress Thermometer
Description
One item scale measuring distress on a scale from 0 to 10. Higer scores indicate higher distress
Time Frame
Baseline, post intervention follow up at 3, 6, and 12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients diagnosed with cancer (all diagnosis). Maximum time since completed treatment at hospital: 12 months Patients are > 18 years of age, able to write/read/speak Norwegian and have their own smart phone or tablet Exclusion Criteria: • None
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lise Solberg Nes, PhD
Organizational Affiliation
Oslo University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Oslo University hospital
City
Oslo
Country
Norway

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
30684438
Citation
Borosund E, Mirkovic J, Clark MM, Ehlers SL, Andrykowski MA, Bergland A, Westeng M, Solberg Nes L. A Stress Management App Intervention for Cancer Survivors: Design, Development, and Usability Testing. JMIR Form Res. 2018 Sep 6;2(2):e19. doi: 10.2196/formative.9954.
Results Reference
derived

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Stress Management Intervention in Early Stage Cancer: Randomized Controlled Trial

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