Cognitive Behavioral Therapy (CBT) for Late Life Anxiety

Sponsor
Wake Forest University Health Sciences (Other)
Overall Status
Recruiting
CT.gov ID
NCT05380115
Collaborator
(none)
10
1
1
21
0.5

Study Details

Study Description

Brief Summary

The purpose of this research study is to assess the acceptability and feasibility of the implementation strategy and fidelity of cognitive-behavioral therapy (CBT) for older adults with Generalized Anxiety Disorder.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Cognitive Behavioral Therapy (CBT)
N/A

Detailed Description

All participants will receive CBT. Each subject will be given a workbook and each chapter in the workbook provides information about a different coping strategy for managing worry and anxiety. There will be a daily assignment in the workbook to complete before a call with the personal study coach. For 10 weeks, participants will have a 45-50 minute session (telephone or video) each week with their study coach. These calls will be confidential. The participant and the personal study coach will review the assigned chapter and completed homework during the weekly telephone sessions. Participants will also fill out questionnaires before starting sessions, when completing all 10 sessions, and 6 months after completing sessions.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
10 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Supportive Care
Official Title:
Implementation of Cognitive-behavioral Therapy for Older Adults With Generalized Anxiety Disorder
Actual Study Start Date :
May 2, 2022
Anticipated Primary Completion Date :
Jul 1, 2023
Anticipated Study Completion Date :
Feb 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: CBT

All subjects enrolled received CBT for 10 weeks.

Behavioral: Cognitive Behavioral Therapy (CBT)
weekly one on one video or telephone interviews with a study coach

Outcome Measures

Primary Outcome Measures

  1. Generalized Anxiety Disorder scale (GAD-7) [Week 11]

    Self-report measure of GAD symptoms. Total scores can range from 0 to 21; higher scores indicate more GAD symptoms.

  2. Penn State Worry Questionnaire-Abbreviated (PSWQ-A) [week 11]

    8-item measure of frequency/intensity of worry; most commonly used worry measure. Scores can range from 8 to 40; higher scores indicate higher levels of worry.

  3. Feasibility-Expectancy Rating Scale [Week 1]

    Assesses beliefs in how logical the treatment received seems, confidence in undergoing treatment/recommending to others, and expectations for success. Used in anxiety treatment studies with older adults. Scores can range from 4 to 40; higher scores indicate more positive expectations.

  4. Feasibility-Intervention adherence [Week 11]

    The percentage of completed sessions

  5. Feasibility-Number of participants who complete at least 75% of sessions [Week 11]

Secondary Outcome Measures

  1. Patient-Reported Outcomes Measurement Information System (PROMIS) [baseline, week 6, week 11]

    8-item measure of general anxiety symptoms; each item is rated on a 5-point scale (1=never; 2=rarely; 3=sometimes; 4=often; and 5=always); scores can range from 8 to 40; higher scores indicate greater severity of anxiety.

  2. Insomnia Sleep Index [baseline, week 6, week 11]

    7-item self-report measure of type and severity of insomnia symptoms. A 5-point Likert scale is used to rate each item (e.g., 0 = no problem; 4 = very severe problem); scores can range from 0 to 28 with higher scores indicating more severe insomnia.

  3. Feasibility-Client Satisfaction Questionnaire [Week 11]

    Assesses satisfaction with treatment. Scores can range from 8 to 32; higher scores indicate more satisfaction.

  4. Feasibility-Working Alliance Inventory, Client [Week 11]

    Assesses therapist-client working alliance. 12 items on a 7-point scale (1=never; 7=always); scores can range from 12 to 84 with higher scores indicating better working relationship.

  5. Feasibility-Working Alliance Inventory, Therapist [Week 11]

    Assesses therapist-client working alliance. 12 items on a 7-point scale (1=never; 7=always); scores can range from 12 to 84 with higher scores indicating better working relationship.

  6. Generalized Anxiety Disorder scale (GAD-7) [Baseline]

    Self-report measure of GAD symptoms. Total scores can range from 0 to 21; higher scores indicate more GAD symptoms.

  7. Generalized Anxiety Disorder scale (GAD-7) [Week 6]

    Self-report measure of GAD symptoms. Total scores can range from 0 to 21; higher scores indicate more GAD symptoms.

  8. Penn State Worry Questionnaire-Abbreviated (PSWQ-A) [baseline]

    8-item measure of frequency/intensity of worry; most commonly used worry measure. Scores can range from 8 to 40; higher scores indicate higher levels of worry.

  9. Penn State Worry Questionnaire-Abbreviated (PSWQ-A) [week 6]

    8-item measure of frequency/intensity of worry; most commonly used worry measure. Scores can range from 8 to 40; higher scores indicate higher levels of worry.

Other Outcome Measures

  1. Healthcare Utilization-Number of Outpatient encounters [Week 37]

  2. Healthcare Utilization-Number of ED visits [Week 37]

  3. Healthcare Utilization-Number of inpatient stays [Week 37]

  4. Healthcare Utilization-Costs for outpatient encounters, ED visits and inpatient stays [Week 37]

  5. Qualitative Interviews [Week 11]

    Analyses will be primarily conducted by Q-PRO

Eligibility Criteria

Criteria

Ages Eligible for Study:
65 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • participants who have had an outpatient visit to an Atrium provider

  • at least one of the following: any diagnosis of an anxiety or depressive disorder; anxiety, depression, or sleep disturbance as a symptom in the problem list or in the note; and use of anxiolytic, anti-depressant, and sleep aide medications.

Exclusion Criteria:
  • diagnosis of dementia or cognitive impairment in the problem list

Contacts and Locations

Locations

Site City State Country Postal Code
1 Atrium Health Wake Forest Baptist Winston-Salem North Carolina United States 27157

Sponsors and Collaborators

  • Wake Forest University Health Sciences

Investigators

  • Principal Investigator: Gretchen Brenes, PhD, Atrium Health Wake Forest Baptist

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Wake Forest University Health Sciences
ClinicalTrials.gov Identifier:
NCT05380115
Other Study ID Numbers:
  • IRB00084483
First Posted:
May 18, 2022
Last Update Posted:
Aug 2, 2022
Last Verified:
May 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Wake Forest University Health Sciences
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 2, 2022