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Feasibility Study Testing a Sleep Intervention in Prostate Cancer Patients With Insomnia

Primary Purpose

Cancer of Prostate, Insomnia

Status
Completed
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
12-week aerobic exercise and cognitive-behavioral therapy
Sponsored by
Danish Cancer Society
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Cancer of Prostate

Eligibility Criteria

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

Inclusion Criteria:

  • Prostate cancer
  • Receiving treatment with androgen deprivation therapy or in combination with chemotherapy
  • Insomnia
  • Over 18-yers old
  • Understand oral and written Danish
  • Written informed consent

Exclusion Criteria:

  • Medical assessment that does not allow aerobic exercise
  • Severe cognitive problems
  • Night work during the interventions period
  • Exercise training more than three times a week

Sites / Locations

  • Oncology Department

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

12-week aerobic exercise and cognitive-behavioral therapy

Control group

Arm Description

12-week aerobic exercise, two times per week, and cognitive-behavioral therapy for insomnia in total four sessions

Patients assigned to the control group will receive usual care

Outcomes

Primary Outcome Measures

Sleep
Measured by actigraphy, to investigate change in sleep from baseline to 12 weeks and the difference in change between intervention - and the control group

Secondary Outcome Measures

Cardiorespiratory fitness
Measured by watt max test, to investigate change from baseline to 12 weeks and the difference in change between intervention and the control group
Fatigue
Measured by the multidimensional fatigue inventory, to investigate change in fatigue from baseline to 12 weeks and 6 months follow up and the difference in change between intervention - and the control group
Physical activity
Measured by the Physical activity Questionnaire to investigate change in physical activity from baseline to 12 weeks and 6 months follow up and the difference in change between intervention - and the control group
Depression
Measured by the Patient Health Questionnaireto, to investigate change in depression from baseline to 12 weeks and 6 months follow up and the difference in change between intervention - and the control group
Anxiety
Measured by the Generalized Anxiety Disorder Questionnaireto, to investigate change in anxiety from baseline to 12 weeks and 6 months follow up and the difference in change between intervention - and the control group
Stress
Measured by Perceived Stress Scale to investigate change in stress from baseline to 12 weeks and 6 months follow up and the difference in change between intervention - and the control group
Quality of life
Measured by European Organization for Research and Treatment Cancer, to investigate change in quality of life from baseline to 12 weeks and 6 months follow up and the difference in change between intervention - and the control group
Sleep quality
Measured by Pittsburgh Sleep Quality Index, to investigate change in sleep quality from baseline to 12 weeks and 6 months follow up and the difference in change between intervention - and the control group
Sleep pattern
Measured by a sleep diary, to investigate change in sleep pattern from baseline to 12 weeks and 6 months follow up and the difference in change between intervention - and the control group
Insomnia
Measured by Insomnia Severity Index, to investigate change in insomnia from baseline to 12 weeks and 6 months follow up and the difference in change between intervention - and the control group
Physical activity
Measured by actigraphy, to investigate change in physical activity from baseline to 12 weeks and the difference in change between intervention - and the control group

Full Information

First Posted
February 9, 2018
Last Updated
May 4, 2020
Sponsor
Danish Cancer Society
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1. Study Identification

Unique Protocol Identification Number
NCT03444532
Brief Title
Feasibility Study Testing a Sleep Intervention in Prostate Cancer Patients With Insomnia
Official Title
Feasibility Study of a Randomized Controlled Trial Testing a Sleep Intervention in Prostate Cancer Patients With Insomnia
Study Type
Interventional

2. Study Status

Record Verification Date
May 2020
Overall Recruitment Status
Completed
Study Start Date
March 2, 2018 (Actual)
Primary Completion Date
March 31, 2019 (Actual)
Study Completion Date
May 31, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Danish Cancer Society

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
This study of a randomized controlled trial aims to evaluate the feasibility of a 12-week sleep program and the randomized controlled trial research procedure. In total 20 participants will be recruited and randomized to the intervention or control group.
Detailed Description
This feasibility study of a randomized controlled trial, aims to evaluate the feasibility of a 12-week sleep program consisting on aerobic exercise and cognitive-behavioral therapy. In this study the investigators wish to evaluate the program as well as the randomized controlled trial research procedure. In total 20 participants will be recruited and randomized to either the intervention group (n=10) or control group (n=10).The intervention group will participate in two exercise sessions each week and four sessions based on cognitive-behavioral therapy for insomnia.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cancer of Prostate, Insomnia

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
12 (Actual)

8. Arms, Groups, and Interventions

Arm Title
12-week aerobic exercise and cognitive-behavioral therapy
Arm Type
Experimental
Arm Description
12-week aerobic exercise, two times per week, and cognitive-behavioral therapy for insomnia in total four sessions
Arm Title
Control group
Arm Type
No Intervention
Arm Description
Patients assigned to the control group will receive usual care
Intervention Type
Behavioral
Intervention Name(s)
12-week aerobic exercise and cognitive-behavioral therapy
Intervention Description
12-week intervention of aerobic exercise training and four session of cognitive-behavioral therapy
Primary Outcome Measure Information:
Title
Sleep
Description
Measured by actigraphy, to investigate change in sleep from baseline to 12 weeks and the difference in change between intervention - and the control group
Time Frame
Change from baseline sleep at 12 weeks
Secondary Outcome Measure Information:
Title
Cardiorespiratory fitness
Description
Measured by watt max test, to investigate change from baseline to 12 weeks and the difference in change between intervention and the control group
Time Frame
Baseline, 12-weeks
Title
Fatigue
Description
Measured by the multidimensional fatigue inventory, to investigate change in fatigue from baseline to 12 weeks and 6 months follow up and the difference in change between intervention - and the control group
Time Frame
Baseline, 12 weeks, 6 month
Title
Physical activity
Description
Measured by the Physical activity Questionnaire to investigate change in physical activity from baseline to 12 weeks and 6 months follow up and the difference in change between intervention - and the control group
Time Frame
Baseline, 12 weeks, 6 month
Title
Depression
Description
Measured by the Patient Health Questionnaireto, to investigate change in depression from baseline to 12 weeks and 6 months follow up and the difference in change between intervention - and the control group
Time Frame
Baseline, 12 weeks, 6 month
Title
Anxiety
Description
Measured by the Generalized Anxiety Disorder Questionnaireto, to investigate change in anxiety from baseline to 12 weeks and 6 months follow up and the difference in change between intervention - and the control group
Time Frame
Baseline, 12 weeks, 6 month
Title
Stress
Description
Measured by Perceived Stress Scale to investigate change in stress from baseline to 12 weeks and 6 months follow up and the difference in change between intervention - and the control group
Time Frame
Baseline, 12 weeks, 6 month
Title
Quality of life
Description
Measured by European Organization for Research and Treatment Cancer, to investigate change in quality of life from baseline to 12 weeks and 6 months follow up and the difference in change between intervention - and the control group
Time Frame
Baseline, 12 weeks, 6 month
Title
Sleep quality
Description
Measured by Pittsburgh Sleep Quality Index, to investigate change in sleep quality from baseline to 12 weeks and 6 months follow up and the difference in change between intervention - and the control group
Time Frame
Baseline, 12 weeks, 6 month
Title
Sleep pattern
Description
Measured by a sleep diary, to investigate change in sleep pattern from baseline to 12 weeks and 6 months follow up and the difference in change between intervention - and the control group
Time Frame
Baseline, 12 weeks, 6 month
Title
Insomnia
Description
Measured by Insomnia Severity Index, to investigate change in insomnia from baseline to 12 weeks and 6 months follow up and the difference in change between intervention - and the control group
Time Frame
Baseline, 12 weeks, 6 month
Title
Physical activity
Description
Measured by actigraphy, to investigate change in physical activity from baseline to 12 weeks and the difference in change between intervention - and the control group
Time Frame
Baseline, 12 weeks

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Prostate cancer Receiving treatment with androgen deprivation therapy or in combination with chemotherapy Insomnia Over 18-yers old Understand oral and written Danish Written informed consent Exclusion Criteria: Medical assessment that does not allow aerobic exercise Severe cognitive problems Night work during the interventions period Exercise training more than three times a week
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Christoffer Johansen, PhD, Dr.Med
Organizational Affiliation
Danish Cancer Society Research Center
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Katrine Løppenthin, PhD
Organizational Affiliation
Danish Cancer Society Research Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Oncology Department
City
Næstved
Country
Denmark

12. IPD Sharing Statement

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Feasibility Study Testing a Sleep Intervention in Prostate Cancer Patients With Insomnia

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