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Effects of Different Aerobic-to-Resistance Training Time Ratios in Adults Aged 50 Years and Older With Prediabetes: A Randomized Controlled Trial

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Record identity and dates

Source
ClinicalTrials.gov
Source record ID
NCT07904962
Title field or adapter rule
{'original_value': 'Effects of Different Aerobic-to-Resistance Training Time Ratios in Adults Aged 50 Years and Older With Prediabetes: A Randomized Controlled Trial', 'source_field': 'protocolSection.identificationModule.officialTitle'}
Ingested At
2026-10-31T23:27:34.374261+00:00
Published At
2026-10-29T00:00:00+00:00
Record Updated At
2026-10-29
Source Retrieved At
2026-10-31T22:18:43.464060+00:00
Timestamp Basis
ClinicalTrials.gov API/RSS response retrieval timestamp recorded by Dossier adapter
Date limitation
ClinicalTrials.gov API/RSS response retrieval timestamp recorded by Dossier adapter

Fields recorded by this source

protocolSection.conditionsModule.conditions
["Prediabetes"]
protocolSection.statusModule.lastUpdatePostDateStruct
{"date": "2026-10-29", "type": "ACTUAL"}
protocolSection.identificationModule.nctId
"NCT07904962"
protocolSection.identificationModule.officialTitle
"Effects of Different Aerobic-to-Resistance Training Time Ratios in Adults Aged 50 Years and Older With Prediabetes: A Randomized Controlled Trial"
protocolSection.statusModule.overallStatus
"NOT_YET_RECRUITING"
protocolSection.designModule.phases
["NA"]
protocolSection.statusModule.resultsFirstPostDateStruct
null

Study condition terms

  • Prediabetes (protocolSection.conditionsModule.conditions)

Interventions recorded in this study

  • {'armGroupLabels': ['Aerobic-to-Resistance 3:1 Training'], 'description': 'Participants will complete 12 weeks of supervised combined aerobic and resistance training, three sessions per week. Each session will include approximately 60 minutes of main training, consisting of approximately 45 minutes of a standardized low-impact aerobic exercise routine and 15 minutes of resistance training. Training intensity and exercise difficulty will be progressively adjusted according to predefined safety criteria and individual tolerance.', 'name': 'Combined Aerobic and Resistance Training (3:1)', 'type': 'BEHAVIORAL'} (protocolSection.armsInterventionsModule.interventions[])
  • {'armGroupLabels': ['Aerobic-to-Resistance 1:1 Training'], 'description': 'Participants will complete 12 weeks of supervised combined aerobic and resistance training, three sessions per week. Each session will include approximately 60 minutes of main training, consisting of approximately 30 minutes of a standardized low-impact aerobic exercise routine and 30 minutes of resistance training. Training intensity and exercise difficulty will be progressively adjusted according to predefined safety criteria and individual tolerance.', 'name': 'Combined Aerobic and Resistance Training (1:1)', 'type': 'BEHAVIORAL'} (protocolSection.armsInterventionsModule.interventions[])
  • {'armGroupLabels': ['Aerobic-to-Resistance 1:3 Training'], 'description': 'Participants will complete 12 weeks of supervised combined aerobic and resistance training, three sessions per week. Each session will include approximately 60 minutes of main training, consisting of approximately 15 minutes of a standardized low-impact aerobic exercise routine and 45 minutes of resistance training. Training intensity and exercise difficulty will be progressively adjusted according to predefined safety criteria and individual tolerance.', 'name': 'Combined Aerobic and Resistance Training (1:3)', 'type': 'BEHAVIORAL'} (protocolSection.armsInterventionsModule.interventions[])
  • {'armGroupLabels': ['Health Education Control'], 'description': 'Participants will receive standardized health education during the 12-week intervention period. The education will provide general information on prediabetes, healthy lifestyles, sleep, smoking and alcohol use, medication adherence, and health and safety. It will not include an individualized structured exercise program or an individualized weight-loss diet prescription.', 'name': 'Standardized Health Education', 'type': 'BEHAVIORAL'} (protocolSection.armsInterventionsModule.interventions[])

An intervention appearing in a study record does not establish an effect or an approved use.

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