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NCT06591325
Twelve Weeks of Resistance Training is Equally As Effective At Improving Cardiovascular Risk Factors in Older Women with and Without Depression: a Non-randomized Cross-over Trial
NA trial testing exercise in Depressive Symptoms in 79 participants. Completed in 25 July 2022.
25 July 2022
Quick facts
| Lead sponsor | Universidade Estadual de Londrina |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | non randomized |
| Design | crossover |
| Masking | none |
| Primary purpose | prevention |
| Enrollment | 79 |
| Start date | 2 November 2021 |
| Primary completion | 25 July 2022 |
| Estimated completion | 25 July 2022 |
| Sites | 1 location across Brazil |
Drugs / interventions tested
- exercise
- Control
Conditions studied
- Depressive Symptoms — all drugs for Depressive Symptoms →
- Aging — all drugs for Aging →
- Resistance Training — all drugs for Resistance Training →
- Cardiovascular Risk Factor — all drugs for Cardiovascular Risk Factor →
Sponsor
Universidade Estadual de Londrina — full company profile →
Who can join
60 and older, female only, with Depressive Symptoms or Aging. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
Background: the purporse was to evaluate and compare the effects of 12 weeks of resistance training (RT) on cardiovascular disease (CVD) risk factors in older women with and without depressive disorders Methods: We included 79 older women, 52 without depressive disorders and 27 with a diagnosis of depressive disorders. The 79 participants passed through 12 weeks of control condition and were instructed to maintain their habitual routine. After the control period, the participants were reevaluated and attended 12 weeks of RT. The Beck Anxiety Inventory (BAI) and Patient Health Questionnaire-9 (PHQ-9) were used to measure anxiety and depressive symptoms, respectively. The serum levels of high-sensitivity C-reactive protein, glucose, total cholesterol (TC), high-density lipoprotein cholesterol (HDL-c), low-density cholesterol (LDL-c), and triglycerides (TG) were used as cardiovascular risk factors. The Linear Mixed Model (LMM) was used to compare between groups.
Publications & conference data
No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.
Verify or expand the search:
- PubMed search for NCT06591325
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
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Other Universidade Estadual de Londrina trials
Trials by the same sponsor.
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT06591325 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Universidade Estadual de Londrina
- Last refreshed: 19 September 2024
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06591325.
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