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Randomized Controlled Trial
. 2015 Oct;72(10):1012-20.
doi: 10.1001/jamapsychiatry.2015.1154.

Telephone-Delivered Cognitive Behavioral Therapy and Telephone-Delivered Nondirective Supportive Therapy for Rural Older Adults With Generalized Anxiety Disorder: A Randomized Clinical Trial

Affiliations
Randomized Controlled Trial

Telephone-Delivered Cognitive Behavioral Therapy and Telephone-Delivered Nondirective Supportive Therapy for Rural Older Adults With Generalized Anxiety Disorder: A Randomized Clinical Trial

Gretchen A Brenes et al. JAMA Psychiatry. 2015 Oct.

Abstract

Importance: Generalized anxiety disorder (GAD) is common in older adults; however, access to treatment may be limited, particularly in rural areas.

Objective: To examine the effects of telephone-delivered cognitive behavioral therapy (CBT) compared with telephone-delivered nondirective supportive therapy (NST) in rural older adults with GAD.

Design, setting, and participants: Randomized clinical trial in the participants' homes of 141 adults aged 60 years and older with a principal or coprincipal diagnosis of GAD who were recruited between January 27, 2011, and October 22, 2013.

Interventions: Telephone-delivered CBT consisted of as many as 11 sessions (9 were required) focused on recognition of anxiety symptoms, relaxation, cognitive restructuring, the use of coping statements, problem solving, worry control, behavioral activation, exposure therapy, and relapse prevention, with optional chapters on sleep and pain. Telephone-delivered NST consisted of 10 sessions focused on providing a supportive atmosphere in which participants could share and discuss their feelings and did not provide any direct suggestions for coping.

Main outcomes and measures: Primary outcomes included interviewer-rated anxiety severity (Hamilton Anxiety Rating Scale) and self-reported worry severity (Penn State Worry Questionnaire-Abbreviated) measured at baseline, 2 months' follow-up, and 4 months' follow-up. Mood-specific secondary outcomes included self-reported GAD symptoms (GAD Scale 7 Item) measured at baseline and 4 months' follow-up and depressive symptoms (Beck Depression Inventory) measured at baseline, 2 months' follow-up, and 4 months' follow-up. Among the 141 participants, 70 were randomized to receive CBT and 71 to receive NST.

Results: At 4 months' follow-up, there was a significantly greater decline in worry severity among participants in the telephone-delivered CBT group (difference in improvement, -4.07; 95% CI, -6.26 to -1.87; P = .004) but no significant differences in general anxiety symptoms (difference in improvement, -1.52; 95% CI, -4.07 to 1.03; P = .24). At 4 months' follow-up, there was a significantly greater decline in GAD symptoms (difference in improvement, -2.36; 95% CI, -4.00 to -0.72; P = .005) and depressive symptoms (difference in improvement, -3.23; 95% CI, -5.97 to -0.50; P = .02) among participants in the telephone-delivered CBT group.

Conclusions and relevance: In this trial, telephone-delivered CBT was superior to telephone-delivered NST in reducing worry, GAD symptoms, and depressive symptoms in older adults with GAD.

Trial registration: clinicaltrials.gov Identifier: NCT01259596.

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Conflict of interest statement

Conflict of Interest Disclosures: None reported.

Figures

Figure 1
Figure 1
CONSORT Flow Diagram a Some participants had multiple reasons for ineligibility. b Telephone-delivered cognitive behavioral therapy (CBT-T) could be completed with between 9 and 11 sessions. Telephone-delivered nondirective supportive therapy (NST-T) required 10 sessions to be complete. c Prespecified primary analysis used all participants with any follow-up data at 2 or 4 months’ follow-up. Those excluded from the prespecified primary analysis did not have any follow-up information. Sensitivity analyses using multiple imputation also were performed to include all participants. d There were 10 total participants missing either the Penn State Worry Questionnaire–Abbreviated (PSWQ-A) or Hamilton Anxiety Rating Scale (HAMA): 2 with the following health problems, 2 indicated they did not have the time, 4 completed the PSWQ-A but not HAMA, and 2 with unknown or other reasons (6 of these participants withdrew consent after providing month 2 data). e Two participants cited self or family health problems, 1 participant cited that he or she did not like randomized therapy, and 1 participant had an unknown reason. f One participant cited health problems and withdrew consent after providing 2-months’ follow-up data. g Two participants cited personal or family health problems and 2 had unknown reasons (2 participants withdrew consent after providing 2-month follow-up data). h Two participants cited health problems.
Figure 2
Figure 2
Treatment Effects on Primary Outcomes
Figure 3
Figure 3
Treatment Effects on Secondary Outcomes

Comment in

References

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