Exercise to Prevent Depression and Anxiety in Older Hispanics
Status: | Completed |
---|---|
Conditions: | Anxiety, Anxiety, Depression |
Therapuetic Areas: | Psychiatry / Psychology |
Healthy: | No |
Age Range: | 60 - Any |
Updated: | 9/9/2018 |
Start Date: | September 2013 |
End Date: | August 2018 |
The study is a randomized pilot trial of a health promotion intervention in the prevention of
anxiety and depression in older Hispanics.
anxiety and depression in older Hispanics.
Eligible participants will be randomized to either the Happy Older Latinos are Active (HOLA)
intervention or a psychoeducation condition. Participants randomized to HOLA will participate
in a group exercise, 3 times a week, for 16 weeks. The exercise is a moderate intensity walk
at a centrally located park in Miami-Dade county and will last for an hour (10 minute
warmup/stretching, 30 minute walk, 5 minute cool down). Groups will consist of 6 participants
and be led by a community health worker. During the cool down phase, participants will plan a
pleasant event to be done in between sessions. Participants randomized to the psychoeducation
component will receive a fotonovela and will meet once a month after they receive the
fotonovela to discuss their thoughts on the materials they received. These discussion groups
will last one hour and will consist of 10 participants. A total of 60 participants will be
randomized (30 to HOLA, 30 to fotonovela). Assessments will be conducted at baseline, post
intervention, 6 months post-intervention, and 12 months post-intervention.
intervention or a psychoeducation condition. Participants randomized to HOLA will participate
in a group exercise, 3 times a week, for 16 weeks. The exercise is a moderate intensity walk
at a centrally located park in Miami-Dade county and will last for an hour (10 minute
warmup/stretching, 30 minute walk, 5 minute cool down). Groups will consist of 6 participants
and be led by a community health worker. During the cool down phase, participants will plan a
pleasant event to be done in between sessions. Participants randomized to the psychoeducation
component will receive a fotonovela and will meet once a month after they receive the
fotonovela to discuss their thoughts on the materials they received. These discussion groups
will last one hour and will consist of 10 participants. A total of 60 participants will be
randomized (30 to HOLA, 30 to fotonovela). Assessments will be conducted at baseline, post
intervention, 6 months post-intervention, and 12 months post-intervention.
Inclusion Criteria:
1. Hispanic (self-identified);
2. Age 60+;
3. Minor depression as defined by a primary DSM-IV Axis I diagnosis of minor depressive
disorder or subthreshold depression defined as a score ≥ 3 on the Patient Health
Questionnaire (PHQ-2), OR subthreshold anxiety as defined as a score ≥ 3 on the
Generalized Anxiety Disorder-2 scale (GAD-2);
4. Absence of episodes of major depression and anxiety disorders for past 12 months (as
determined by the MINI);
5. Voluntary informed consent for participation in the study by the participant or by the
participant's legally designated guardian or conservator;
6. Medical clearance for participation in an exercise program by a physician, physician's
assistant, or nurse practitioner;
7. Expect to be resident in Miami for the subsequent 12 months.
Exclusion Criteria:
1. Currently residing in a nursing or group home;
2. A terminal physical illness expected to result in the death within one year;
3. A diagnosis of dementia, co-morbid diagnosis of dementia, or significant cognitive
impairment as indicated by an MMSE score <24;
4. Presence of any axis 1 psychiatric disorder or substance abuse during preceding 12
months;
5. History of psychiatric disorders other than non-psychotic unipolar major depression or
anxiety disorder;
6. High suicide risk, i.e., intent or plan to attempt suicide in the near future (a
response of "yes" to questions 3, 4, and/or 5 on the Paykel Questionnaire);
7. Participants taking cognitive enhancing medication or psychotropic medications (e.g.
antidepressants);
8. unable to complete 400 m walk test in less than 15 min;
9. if participant heart rate exceeded 170 beats per minute OR systolic blood pressure
exceeds 180 during 400 m walk test;
10. chest or leg pain, dyspnea, dizziness, feeling faint, or other significant symptoms
while completing 400 m walk test;
(i) acute or severe medical illness that would prevent participants from walking at a
moderate pace for 45 minutes, three times a week.
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