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Late life intervention to improve function in elderly patients with depression

Does a home-based physical activity programme improve function and depressive symptomatology in older primary care patients: a randomised controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12605000475640
Acronym
DeLLITE
Enrollment
190
Registered
2005-09-23
Start date
2006-03-26
Completion date
Unknown
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

Interventions

A trained research nurse conducts a functional assessment Participant identifies a functional goal (with the assistance of the COPM) Research nurse designs an individualised home-based physical activity programme based on attaining the functional goal The intervention will be an adaptation of the Otago Exercise Programme - regular walking, three times weekly, progressive resistance training of lower leg strengthening using weights, and balance retraining using progressive balance exercises â¿¿

A trained research nurse conducts a functional assessment Participant identifies a functional goal (with the assistance of the COPM) Research nurse designs an individualised home-based physical activity programme based on attaining the functional goal The intervention will be an adaptation of the Otago Exercise Programme - regular walking, three times weekly, progressive resistance training of lower leg strengthening using weights, and balance retraining using progressive balance exercises â¿¿ with the addition of arm strengthening exercises and tai chi exercises for balance. Social contact will be encouraged by involvement of an exercise and walking companion. The intervention nurse will visit on weeks 0, 1, 2, 4, 5, 8, and 12 (3 months) to ensure adherence and progression of activity. Participants will be encouraged to maintain the programme independently up to a total of 12 months.

Sponsors

Health Research Council of NZ
Lead SponsorGovernment body

Study design

Allocation
Randomised controlled trial
Intervention model
Single group
Primary purpose
Prevention
Masking
Blinded (masking used)

Eligibility

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

Inclusion criteria

Eligible patients include those able to communicate in English, and screened as suffering from depression. Patients who are already on pharmacotherapy for depression will be eligible to participate in the trial.

Exclusion criteria

Patients will be excluded if they suffer from dementia, terminal illness or an unstable cardiac condition, are unable to communicate in English, or are not living in Auckland permanently.

Outcome results

None listed

Source: ANZCTR · Data processed: Apr 5, 2026