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Randomised Control Trial of the Effectiveness of Exercise Augmentation in Patients with Post Traumatic Stress Disorder

In people with primary Post Traumatic Stress Disorder (PTSD) what is the effect of exercise in addition to usual care, on PTSD symptoms and physical parameters compared to usual care only: A Randomised Control Trial.

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12610000579099
Acronym
REAPP
Enrollment
80
Registered
2010-07-19
Start date
2010-10-15
Completion date
2012-05-01
Last updated
2020-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Brief summary

This study will investigate the effects of a 12 week individualised exercise program on PTSD symptoms, physical parameters such as blood pressure, sleep patterns and medication useage. It is hypothesized that by adding this structured exercise program to usual care, patient outcomes will improve.

Interventions

Participants randomised to the intervention group will complete a 12 week individualised exercise program based around the Randomised Exercise Augmentation for PTSD Patients (REAPP) exercises, involving exercise bands and body weight as resistance. Participants will have one supervised session of approximately 30 minutes duration per week and will be asked to complete an additional two unsupervised sessions per week of approximately the same duration. Exercises are mostly compound, and focus on

Participants randomised to the intervention group will complete a 12 week individualised exercise program based around the Randomised Exercise Augmentation for PTSD Patients (REAPP) exercises, involving exercise bands and body weight as resistance. Participants will have one supervised session of approximately 30 minutes duration per week and will be asked to complete an additional two unsupervised sessions per week of approximately the same duration. Exercises are mostly compound, and focus on the major muscle groups. A walking component will also be included within the intervention. All sessions will be held at St John of God Healthcare's Richmond Hospital and will be supervised by an Exercise Physiologist or a nurse trained in delivering the exercise program. Motivational interviewing, goal setting and exercise diaries will be used in order to facilitate adherence and encourage adoption of the intervention program.

Sponsors

Dr Simon Rosenbaum
Lead SponsorIndividual

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Blinded (masking used)

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Diagnositc and Statistical Manual of Mental Disorders-IV (DSM)diagnosis of PTSD Medically fit to participate in an exercise program Physically capable of exercising Competent to consent to participate in research as determined by medical staff

Exclusion criteria

Medically unfit to participate in an exercise program Pregnant or planning pregnancy within the next year. Complex PTSD with trauma occurring in childhood only.

Outcome results

None listed

Source: ANZCTR · Data processed: Mar 28, 2026