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Anxiety With Cancer in the Elderly (ACE): A Cognitive-behavioral Intervention

Primary Purpose

Anxiety, Depression, Quality of Life

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Managing Anxiety from Cancer (MAC)
Sponsored by
Memorial Sloan Kettering Cancer Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional supportive care trial for Anxiety focused on measuring Cancer, Anxiety, Cognitive behavior therapy, Elderly, Caregivers

Eligibility Criteria

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

Inclusion Criteria:

  1. Patient age 65 years or older
  2. Diagnosis of cancer
  3. Patient and/or caregiver score of 8 or higher on the anxiety subscale of the Hospital Anxiety and Depression Scale
  4. A primary informal caregiver who is willing and able to participate
  5. Patient and caregiver are able to communicate over the telephone
  6. Caregiver is age 21 years or older.

Exclusion Criteria:

  1. Patient or caregiver is not fluent in English
  2. Patient or caregiver is too weak or cognitively impaired to participate in the intervention
  3. Patient or caregiver has received CBT since the patient's cancer diagnosis
  4. Patient or caregiver has an active major psychiatric condition such as schizophrenia
  5. Patient only experiences anxiety in the context of a specific medical procedure
  6. Patient or caregiver endorses active suicidal ideation

Sites / Locations

  • Weill Medical College of Cornell University

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Managing Anxiety from Cancer (MAC)

Arm Description

Older adults with cancer and their primary informal caregiver will receive a six-session cognitive-behavior therapy intervention administered over the telephone by a trained study interventionist. The intervention is administered weekly and each session is 45-50 minutes in length. Patients and caregivers will receive the intervention independently and from separate therapists.

Outcomes

Primary Outcome Measures

Intervention feasibility
Attrition rates
Intervention acceptability
Likert scale ratings of perceived helpfulness and readability of the intervention
Patient/caregiver adherence
Sum of number of intervention exercises completed with number of sessions completed by patients and caregivers

Secondary Outcome Measures

Change in anxiety from baseline to post-intervention
Anxiety sub-scale of the Hospital Anxiety and Depression Scale
Change in distress from baseline to post-intervention
Distress Thermometer
Emotional health-related quality of life
Functional Assessment of Cancer Therapy-General: Emotional Quality of Life Sub-Scale; Caregiver Quality of Life-Cancer
Change in depression from baseline to post-intervention
Depression sub-scale of the Hospital Anxiety and Depression Scale

Full Information

First Posted
April 12, 2016
Last Updated
October 9, 2020
Sponsor
Memorial Sloan Kettering Cancer Center
Collaborators
Weill Medical College of Cornell University
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1. Study Identification

Unique Protocol Identification Number
NCT02747160
Brief Title
Anxiety With Cancer in the Elderly (ACE): A Cognitive-behavioral Intervention
Official Title
Evaluation of an Anxiety Intervention for Older Adults With Cancer and Informal Caregivers of Older Adults With Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
October 2020
Overall Recruitment Status
Completed
Study Start Date
June 2016 (Actual)
Primary Completion Date
July 2, 2020 (Actual)
Study Completion Date
July 2, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Memorial Sloan Kettering Cancer Center
Collaborators
Weill Medical College of Cornell University

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The purpose of this study is to examine the feasibility and acceptability of and patient adherence to a telephone-administered cognitive-behavioral therapy intervention for anxiety in older adults (65 years and older) with cancer and their primary informal caregiver. This study will also examine whether the intervention has a clinically significant impact on patient anxiety (primary outcome) and depression, distress, and quality of life (secondary outcomes).
Detailed Description
This study is a single arm pre-post evaluation of a six-session telephone-administered cognitive-behavioral therapy (CBT) intervention for anxiety in older adults with cancer and their primary informal (unpaid) caregiver. The primary purposes of this study are to evaluate the feasibility of the intervention and study procedures, acceptability of the intervention to older adults with cancer and their primary informal caregiver, and patient and caregiver adherence to the intervention. The secondary purpose is to examine changes in patient and caregiver anxiety, depression, distress, and quality of life pre to post intervention to determine whether the intervention has a clinically significant impact on these outcomes. Anxiety is the primary outcome; depression, distress, and quality of life are secondary outcomes. Patients will be 65 years of age or older and will be recruited from the myeloma, lung, lymphoma, gynecologic, and gastrointestinal cancer clinics at a single institution. Study measures will be administered by telephone prior to initiating the intervention (pre-intervention) and following intervention completion (post-intervention).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Anxiety, Depression, Quality of Life
Keywords
Cancer, Anxiety, Cognitive behavior therapy, Elderly, Caregivers

7. Study Design

Primary Purpose
Supportive Care
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
50 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Managing Anxiety from Cancer (MAC)
Arm Type
Experimental
Arm Description
Older adults with cancer and their primary informal caregiver will receive a six-session cognitive-behavior therapy intervention administered over the telephone by a trained study interventionist. The intervention is administered weekly and each session is 45-50 minutes in length. Patients and caregivers will receive the intervention independently and from separate therapists.
Intervention Type
Behavioral
Intervention Name(s)
Managing Anxiety from Cancer (MAC)
Intervention Description
The intervention consists of six telephone-administered sessions. Session topics include psychoeducation on anxiety, behavioral strategies for managing anxiety, cognitive restructuring, communication skills training, acceptance techniques (patient only), problem-solving strategies (caregiver only), and planning for future anxiety. Session content is tailored for older adults and caregivers of older adults with cancer.
Primary Outcome Measure Information:
Title
Intervention feasibility
Description
Attrition rates
Time Frame
Post-intervention (6-8 weeks after baseline)
Title
Intervention acceptability
Description
Likert scale ratings of perceived helpfulness and readability of the intervention
Time Frame
Post-intervention (6-8 weeks after baseline)
Title
Patient/caregiver adherence
Description
Sum of number of intervention exercises completed with number of sessions completed by patients and caregivers
Time Frame
Post-intervention (6-8 weeks after baseline)
Secondary Outcome Measure Information:
Title
Change in anxiety from baseline to post-intervention
Description
Anxiety sub-scale of the Hospital Anxiety and Depression Scale
Time Frame
Baseline (1-2 weeks after enrollment) and Post-intervention (6-8 weeks after baseline)
Title
Change in distress from baseline to post-intervention
Description
Distress Thermometer
Time Frame
Baseline (1-2 weeks after enrollment) and Post-intervention (6-8 weeks after baseline)
Title
Emotional health-related quality of life
Description
Functional Assessment of Cancer Therapy-General: Emotional Quality of Life Sub-Scale; Caregiver Quality of Life-Cancer
Time Frame
Baseline (1-2 weeks after enrollment) and Post-intervention (6-8 weeks after baseline)
Title
Change in depression from baseline to post-intervention
Description
Depression sub-scale of the Hospital Anxiety and Depression Scale
Time Frame
Baseline (1-2 weeks after enrollment) and Post-intervention (6-8 weeks after baseline)

10. Eligibility

Sex
All
Minimum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patient age 65 years or older Diagnosis of cancer Patient and/or caregiver score of 8 or higher on the anxiety subscale of the Hospital Anxiety and Depression Scale A primary informal caregiver who is willing and able to participate Patient and caregiver are able to communicate over the telephone Caregiver is age 21 years or older. Exclusion Criteria: Patient or caregiver is not fluent in English Patient or caregiver is too weak or cognitively impaired to participate in the intervention Patient or caregiver has received CBT since the patient's cancer diagnosis Patient or caregiver has an active major psychiatric condition such as schizophrenia Patient only experiences anxiety in the context of a specific medical procedure Patient or caregiver endorses active suicidal ideation
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kelly M Trevino, PhD
Organizational Affiliation
Weill Medical College of Cornell University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Weill Medical College of Cornell University
City
New York
State/Province
New York
ZIP/Postal Code
10065
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Anxiety With Cancer in the Elderly (ACE): A Cognitive-behavioral Intervention

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