Project UPLIFT to Reduce Anxiety and Depression in CF Patients

Depression Clinical Trial

Official title:

Project UPLIFT to Reduce Anxiety and Depression in CF Patients

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03139266
• Other study ID #: HM20002923
• Secondary ID: SCHECH15A0
• Status: Completed
• Phase: N/A
• Start date: April 7, 2015
• Est. completion date: August 2, 2022

Study information

• Verified date: June 2023
• Source: Virginia Commonwealth University
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

People with CF have elevated rates of anxiety and depression when compared to the general population. Anxiety and depression can have a negative impact on adherence and disease self-management, leading to worse CF health outcomes such as respiratory symptoms, functional capacity, and health-related quality of life (HRQOL).

Project UPLIFT is a group mental health intervention that can be delivered by telephone or Web, though for this study the intervention will be web based only. Project UPLIFT was originally developed as a depression treatment and prevention program for people with epilepsy and was shown to be effective in reducing depression and increasing knowledge and skills. Recently, Project UPLIFT was revised to help people with CF manage their depression and anxiety and shown to be apparently successful in a pilot study that included adolescents and adults with CF.

The goals of this project are to determine the effectiveness of Project UPLIFT in reducing anxiety and depression in adolescents and adults with CF, as well as increasing their quality of life and other physical health-related disease outcomes.

Description:

The Project UPLIFT intervention was designed for delivery to groups of six to eight people by telephone or Internet, though for this study the intervention will be web based only. The telephone intervention comprised eight hour-long sessions, each including check-in, instruction, skill building, and discussion, with homework between sessions. The Web intervention contains the same elements: check-in, video instruction, skill building, a discussion board, and homework between sessions. Instruction focuses on increasing knowledge about depression, CF, CBT, and mindfulness and skills related to CBT and mindfulness. Participation in the sessions involves skills practice, discussions, and group exercises based on the sessions' main topics. CBT-related topics include thought monitoring, identifying cognitive distortions, self-esteem, problem identification, goal setting, and identifying supports. Relaxation exercises, including a body scan (i.e., a mindfulness exercise) and progressive muscle relaxation, are also used for coping and to facilitate awareness of the body. Mindfulness activities include attention to skin, sights, and sounds and other meditations. Participants will practice their skills between sessions through homework assignments including monitoring and changing thoughts, and practicing relaxation exercises, meditation exercises, and mindfulness. A week's homework is discussed at the beginning of the next session. The program is designed to guide participants from noticing, challenging, and changing thoughts (CBT components), to staying in the present moment with acceptance of and nonreactivity to those thoughts (mindfulness components). All sessions will be co-facilitated by a layperson with CF and a doctoral student in psychology, supervised by a licensed clinical psychologist.

Once the subjects are recruited and enrolled, baseline assessment will take place and then they will be randomized into the intervention group or treatment-as-usual control group condition (recommendation to consider obtaining mental health services). All participants will complete questionnaires via the internet. Following the initial assessment, the groups will receive their assigned intervention (or control treatment) and there will be questionnaire based testing of mental health, QoL, and disease management at 2 months (immediately following the group intervention), 6 months, and 12 months.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 85
• Est. completion date: August 2, 2022
• Est. primary completion date: August 2, 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: 13 Years and older

Eligibility

*Please note that only patients who are seen by one of our participating CF clinics (listed in "locations") will be approached about UPLIFT (if eligible) during this phase of the UPLIFT project.*

Inclusion Criteria:

First, patients will have to agree to have their contact information shared with the study team in order to be eligible.

Eligibility criteria:

• have been diagnosed with CF for at least 1 year;

• score 5-14 on the GAD-7 and/or a 5-19 on the PHQ-9;

• be =13 years of age;

• be English speaking; and

• not have a prominent cognitive impairment.

Exclusion Criteria:

• Persons reporting active suicidal ideation on the PHQ-9 will be excluded.

Related Conditions & MeSH terms

• Anxiety
• Anxiety Disorders
• Cystic Fibrosis
• Depression
• Depressive Disorder
• Fibrosis

Intervention

Behavioral:
• UPLIFT
Participation in the sessions involves skills practice, discussions, and group exercises based on the sessions' main topics. CBT-related topics include thought monitoring, identifying cognitive distortions, self-esteem, problem identification, goal setting, and identifying supports. Relaxation exercises, including a body scan (i.e., a mindfulness exercise) and progressive muscle relaxation, are also used for coping and to facilitate awareness of the body. Mindfulness activities include attention to skin, sights, and sounds and other meditations. Participants will practice their skills between sessions through homework assignments including monitoring and changing thoughts, and practicing relaxation exercises, meditation exercises, and mindfulness.
• Treatment as usual
The control group will receive the recommendation to consider maintaining mental health services

Locations

Country	Name	City	State
United States	Virginia Commonwealth University	Richmond	Virginia

Sponsors (8)

Lead Sponsor	Collaborator
Virginia Commonwealth University	Boston Children's Hospital, Children's Hospital Medical Center, Cincinnati, Cystic Fibrosis Foundation, Emory University, Johns Hopkins University, University at Buffalo, University of Michigan

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	(Exploratory) Change in CF disease severity status.	CF disease related measures will be collected from routine clinic visits that occur from the time of enrollment to final UPLIFT follow-up	Baseline (at 0 week), Tx End (at 8 weeks), Follow-up (at 6 months post Tx End), Extended Follow-up (at 12 months post Tx End)
Primary	Reduce symptoms of anxiety among UPLIFT Tx Group participants.	Anxiety symptoms will be assessed with the Generalized Anxiety Disorder-7 (GAD-7)	Baseline (at 0 week), Tx End (at 8 weeks), Follow-up (at 6 months post Tx End), Extended Follow-up (at 12 months post Tx End)
Primary	Reduce symptoms of depression among UPLIFT Tx Group participants.	Depressive Symptoms will be assessed with the Patient Health Questionnaire-9 (PHQ-9).	Baseline (at 0 week), Tx End (at 8 weeks), Follow-up (at 6 months post Tx End), Extended Follow-up (at 12 months post Tx End)
Secondary	Increase quality of life among UPLIFT Tx Group participants.	Quality of Life will be assessed using the Cystic Fibrosis Questionnaire-Revised (CFQ-R).	Baseline (at 0 week), Tx End (at 8 weeks), Follow-up (at 6 months post Tx End), Extended Follow-up (at 12 months post Tx End)
Secondary	Increase satisfaction with life among UPLIFT Tx Group participants.	Satisfaction with life will be measured using the Satisfaction with Life Scale.	Baseline (at 0 week), Tx End (at 8 weeks), Follow-up (at 6 months post Tx End), Extended Follow-up (at 12 months post Tx End)
Secondary	Improve knowledge and skills regarding self-management of anxiety and depression among UPLIFT Tx Group participants.	Will be assessed using an 18-item true-false measure developed during the development of Project UPLIFT.	Baseline (at 0 week), Tx End (at 8 weeks), Follow-up (at 6 months post Tx End), Extended Follow-up (at 12 months post Tx End)
Secondary	Increase self-efficacy among UPLIFT Tx Group participants.	We will measure this using the Depression Coping Self-Efficacy Scale (DCSES).	Baseline (at 0 week), Tx End (at 8 weeks), Follow-up (at 6 months post Tx End), Extended Follow-up (at 12 months post Tx End)