Quality of Life Clinical Trial
Official title:
Comparison of Low-dose Maximal-intent Versus Controlled-tempo Resistance Training on Quality-of-life, Functional Capacity, and Strength in Untrained Healthy Adults: a Randomised Controlled Trial
| NCT number | NCT06107855 |
| Other study ID # | 45459 |
| Secondary ID | |
| Status | Completed |
| Phase | N/A |
| First received | |
| Last updated | |
| Start date | August 1, 2022 |
| Est. completion date | March 29, 2023 |
| Verified date | October 2023 |
| Source | Northumbria University |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
The aims of this study were to: 1. Compare the effects of low-dose Maximal Intent and Controlled Tempo Resistance Training on untrained healthy adults' quality-of-life, functional capacity, and strength. 2. Qualitatively explore perceptions of Maximal Intent and Controlled Tempo Resistance Training.
| Status | Completed |
| Enrollment | 20 |
| Est. completion date | March 29, 2023 |
| Est. primary completion date | March 29, 2023 |
| Accepts healthy volunteers | Accepts Healthy Volunteers |
| Gender | All |
| Age group | 30 Years to 59 Years |
| Eligibility | Inclusion Criteria: - Participants were eligible if they were between 30-60 years old - Uninjured - Had no cardiovascular or neuromuscular conditions - Had not participated in lower-limb RT in the previous six months. Exclusion Criteria: - Participants were excluded if they had either taken part in any lower-limb RT in the last six months - Had underlying health condition(s) that prevented them from participating in RT - Regularly met or exceeded the UK recommended PA guideline of 150-minutes of moderate to intense PA per week. |
| Country | Name | City | State |
|---|---|---|---|
| United Kingdom | Nortuhmbria University | Newcastle | Tyne And Wear |
| Lead Sponsor | Collaborator |
|---|---|
| Northumbria University |
United Kingdom,
Pearson LT, Behm DG, Goodall S, Mason R, Stuart S, Barry G. Effects of maximal-versus submaximal-intent resistance training on functional capacity and strength in community-dwelling older adults: a systematic review and meta-analysis. BMC Sports Sci Med Rehabil. 2022 Jul 16;14(1):129. doi: 10.1186/s13102-022-00526-x. — View Citation
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | Quality-of-life | Participant quality of life (focus group questions & SF-36) | The time frame for my testing intervals will be conducted at specific time points: at baseline, Week 1, Week 4, and Week 9, out of a total study duration of 9 weeks. | |
| Secondary | Balance | Using the biodex SD to do a 3 x 20s double-foot eyes-open balance test on Level 6. | The time frame for my testing intervals will be conducted at specific time points: at baseline, Week 1, Week 4, and Week 9, out of a total study duration of 9 weeks. | |
| Secondary | 6-minute Walk Test (6MWT) | a "brisk"-paced 6-minute walk test. | The time frame for my testing intervals will be conducted at specific time points: at baseline, Week 1, Week 4, and Week 9, out of a total study duration of 9 weeks. | |
| Secondary | Timed-up-and-go (TUG) | Standing from a chair, walking to a point 3 metres away, turn, and return to the chair as quick as possible whilst walking. | The time frame for my testing intervals will be conducted at specific time points: at baseline, Week 1, Week 4, and Week 9, out of a total study duration of 9 weeks. | |
| Secondary | 30-second sit-to-stand (30s-STS) | Maximal amount of repetitions a participant can stand up from a chair in 30-seconds. | The time frame for my testing intervals will be conducted at specific time points: at baseline, Week 1, Week 4, and Week 9, out of a total study duration of 9 weeks. | |
| Secondary | Strength (1RM) | Participants one-repetition max on leg press | The time frame for my testing intervals will be conducted at specific time points: at baseline, Week 1, Week 4, and Week 9, out of a total study duration of 9 weeks. | |
| Secondary | BMI | Additional measures calculated from participants test results | The time frame for my testing intervals will be conducted at specific time points: at baseline, Week 1, Week 4, and Week 9, out of a total study duration of 9 weeks. | |
| Secondary | Strength-to-mass | Additional measures calculated from participants test results | The time frame for my testing intervals will be conducted at specific time points: at baseline, Week 1, Week 4, and Week 9, out of a total study duration of 9 weeks. |
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|---|---|---|---|
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