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UPLIFT: Progressive Resistance Training (PRT) as Adjunctive Treatment for Alcohol Use Disorder (AUD)

Progressive Resistance Training as an Adjunct Treatment for Alcohol Use Disorder

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12621001689864
Enrollment
32
Registered
2021-12-10
Start date
2022-02-01
Completion date
Unknown
Last updated
2021-12-21

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

Conditions

None listed

Brief summary

The primary aims of this project are to determine the effects of high intensity progressive resistance training (PRT) on the number of alcoholic drinks consumed per week, measured using a 7-day recall in adults who have undergone rehabilitation for alcohol use disorder with mental health comorbidities. Participants will be randomised to receive either PRT, 3 days per week for 12 weeks after discharge into the outpatient program in addition to usual care provided in the outpatient program at St John of God (Burwood) Hospital, or usual care in the outpatient program only at St John of God (Burwood) Hospital. Participants randomised to the control intervention will receive usual care in the 12-week Alcohol, Drugs and Addictive Behaviours outpatient program at St John of God (Burwood) Hospital. We will not advise on treatment. Blinded assessments will occur pre-, and post intervention. Unequal randomisation will be used to minimise drop-out rates, in a ratio of 2 participants randomised to the intervention group and 1 to the control group. For this trial we have conservatively estimated an effect size of 1.1. With a beta 0.8 and alpha of 0.05, a total of 32 participants will need to be recruited, 11 participants in the control group and 21 in the intervention group, to show significant effects for the number of drinks consumed per week.

Interventions

Interventional Description of intervention(s) / exposure 1.Brief Name: High intensity progressive resistance training (PRT) in addition to usual care (please see description of usual care received by the control group). 2.Rationale: PRT or strength training has been reported as the preferred modality of exercise by individuals undergoing substance abuse treatment (Abrantes et al, 2011). To date, only one study of high intensity PRT has been published, and it was found to be superior to aerobic e

Interventional Description of intervention(s) / exposure 1.Brief Name: High intensity progressive resistance training (PRT) in addition to usual care (please see description of usual care received by the control group). 2.Rationale: PRT or strength training has been reported as the preferred modality of exercise by individuals undergoing substance abuse treatment (Abrantes et al, 2011). To date, only one study of high intensity PRT has been published, and it was found to be superior to aerobic exercise and moderate intensity resistance training (circuit training) in reducing depressive symptoms during rehabilitation for alcohol and substance abuse (Palmer et al, 1995). This is in agreement with the known anti-depressant effects of PRT (Gordon et al, 2018; Cooney et al, 2013; Herring et al, 2012; Singh et al, 2005). However, the effect of PRT on alcohol dependency itself are currently unknown, and so PRT presents a novel and innovative therapy that warrants testing in appropriately designed studies. 3. Materials: Free-weights and Digital K400 Keiser pneumatic resistance machines (Keiser Sports health Equipments, Inc. Fresno, CA) 4. PRT Protocol: The intervention period is 12 weeks in duration and training will be 3 times per week for approximately 45-60 minutes. Week 1 of the intervention will include familiarisation and gradual increase in target intensity from 50%, 60%, 70% 1RM in each successive session. From the first session of week 2, training intensity will be set at 80% 1RM and progressed by a projected gain in strength of 3% 1RM each session, used in conjunction with the Borg Rating of Perceived Exertion Scale. At the start of every 7th session, 1RM will be re-tested and target weight at 80% 1RM will be recalculated based on the new 1RM. Total training volume is 24 repetitions per exercise, set initially at 3 sets of 8 repetitions. However, as intensity is most important, sets and repetitions may be manipulated such that prescribed intensity is adhered to and the total volume remains 24 repetitions per exercise. In addition, assessor observation of pain, accessory muscle use or violations of form will be used to titrate the load. Eight resistance machines will be used and exercises will be completed in the following order; leg press, seated row, knee extension, chest press, knee flexion, tricep pushdown, lateral raises and plantar flexion initially. There will be 2-3 minutes rest between sets to allow sufficient recovery of anaerobic metabolism. 5. Supervision: Subjects will be trained by an exercise physiologist accredited by Exercise and Sport Science Australia in a supervised setting at a ratio of 1 trainer for 4-5 subjects 6. Mode of delivery: Every training session will be supervised face to face. 7. Location: Once patients are discharged into the outpatient program, participants randomly assigned to the intervention group will commence their training at the Faculty of Health Science, Cumberland Campus of the University of Sydney in Lidcombe NSW Australia. 8. Frequency: Participants will train 3 days of the week on non-consecutive days over the 12-week intervention period. 9. Adherence: Session adherence and compliance to the exercise prescription will also be monitored and recorded. Participants will be contacted following any missed sessions, to discuss reasons for absence and to encourage their attendance at subsequent training sessions. Abrantes, A.M., Battle, C.L., Strong, D.R., Ing, E., Dubreuil, M.E., Gordon, A., & Brown, R.A.(2011). Exercise preferences of patients in substance abuse treatment. Mental Health and Physical Activity, 4(2), 79-87. Cooney, GM., Dwan, K., Greig, CA., Lawlor, DA., Rimer, J., Waugh, FR., & McMurdo, M. (2013). Exercise for depression. Cochrane Database of Systematic Reviews, (9) Cd004366. Gordon, BR., McDowell, CP., Hallgren, M., Meyer, JD., Lyons, M., & Herring, MP. (2018). Association of Efficacy of Resistance Exercise Training With Depressive Symptoms: Meta-analysis and Meta-regression Analysis of Randomized Clinical Trials. JAMA Psychiatry, 75(6), 566-576 Herring, MP., Puetz, TW., O’Connor, PJ., & Dishman, RK. (2012). Effect of exercise training on depressive symptoms among patients with a chronic illness: a systematic review and meta-analysis of randomized controlled trials. JAMA Internal Medicine, 172(2), 101-111 Palmer, J.A., Palmer, L.K., Michiels, K., & Thigpen, B. (1995). Effects of type of exercise on depression in recovering substance abusers. Perceptual and Motor Skills, 80, 523-530. Singh, N.A., Stavrinos, T.M., Scarbek, Y., Galambos, G., Liber, C., & Fiatarone Singh, MA. (2005). A randomized controlled trial of high versus low intensity weight training versus general practitioner care for clinical depression in older adults. The Journals of Gerontology. Series A, Biological Sciences and Medical Sciences, 60(6):768-776.

Sponsors

the University of Sydney
Lead SponsorUniversity

Study design

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

Eligibility

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

Inclusion criteria

We will recruit men and women, aged 18+, admitted to St John of God (Burwood) hospital, for treatment of an alcohol use disorder. Participants must also have a current co-morbid mental health condition (other than active psychosis). This will be confirmed in one of the following ways: - Identified when auditing medical records at St John of God Hospital. - Current pharmacological treatment for a mental health condition identified when auditing medical records, - Confirmed by general practitioner or psychiatrist. Individuals who do not satisfy either of the criteria above, may be eligible for inclusion based on a score of greater than 10 on the PHQ-9 (major depressive disorder) or a score greater than 10 on the GAD-7 (anxiety). Diagnosis of depression or anxiety will be confirmed by the study physician. Participants must have completed acute withdrawal treatment for the alcohol or any other substance they have been using before they are approached for recruitment. Participants must have the capacity to consent (assessed by SJoGH admitting staff), competency in English sufficient for assessment and training, and clearance from the study physician to exercise.

Exclusion criteria

Participants will be excluded from participation in the study if they present with active suicidal ideation, active psychosis, delirium, dementia, acute withdrawal, unstable cardiovascular disease, unrepaired aortic aneurysm, rapidly progressive or terminal illness and other conditions that would preclude participation in an exercise trial or require urgent psychiatric referral. Participants who are performing greater than 150 minutes per week of moderate intensity or greater intensity planned exercise of any kind, will also be excluded from participation.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026