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NCT07446231
Reframing Retirement: An Examination of Identity Change and Self-Regulation Approaches to Promote Physical Activity
NA trial testing Self Regulation Digital Health Online Platform in Physical Activity in 159 participants. Not yet recruiting.
31 March 2030
Quick facts
| Lead sponsor | University of Victoria |
|---|---|
| Phase | NA |
| Status | Not yet recruiting |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | single |
| Primary purpose | prevention |
| Enrollment | 159 |
| Start date | 1 March 2026 |
| Primary completion | 31 March 2030 |
| Estimated completion | 31 March 2030 |
| Sites | 1 location across Canada |
Drugs / interventions tested
- Self Regulation Digital Health Online Platform
- Identity Digital Health Online Platform
- Control Digital Health Online Platform
Conditions studied
- Physical Activity — all drugs for Physical Activity →
- Health Promotion — all drugs for Health Promotion →
Sponsor
University of Victoria
Who can join
Adults 60 to 70, any sex, with Physical Activity or Health Promotion. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The primary objective of this clinical trial is to test the efficacy of an innovative multimodal eHealth \& mHealth intervention (focused on emphasizing identity/habit and/or self-regulation) on increasing moderate to vigorous (MVPA) across 12 months among newly retired adults not meeting Physical Activity guidelines at study baseline, thus at higher risk of age-related chronic diseases. The secondary objectives are to examine whether these approaches improve physical and mental well-being and health related fitness-outcomes. Principal Research Question 1: Does an intervention focused on identity/habit + self-regulation skills + education (ID) increase moderate-to-vigorous intensity physical activity (MVPA) compared with an intervention focused on self-regulation skills + education (SR), and an education control condition (ED)? Three-arm parallel design single blinded randomized controlled trial. Participants will be randomized to one of three groups (ID, SR, ED) for 12 months duration. * After the initial screening process, eligible participants will be provided with an accelerometer-mailed or delivered in person-to wear for seven consecutive days. Data collected will verify baseline physical activity levels and determine final eligibility based on adherence to physical activity guideline thresholds. * Participants will visit the lab for fitness testing and complete an online questionnaire See below in "detailed description" the breakdown/delivery given for each of the 3 arms.
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
Verify or expand the search:
- PubMed search for NCT07446231
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Related trials
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Currently open trials in the same condition.
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- NCT07415460 — Evaluating the Impact of SKY Breath Meditation on Stress, Well-being, and Connection in College Students · NA · recruiting
- NCT07585409 — Physical Activity in Persons With Parkinson's Disease · recruiting
Other University of Victoria trials
Trials by the same sponsor.
- NCT06098716 — All in the Family: Promoting Family Function Through Physical Activity · NA · recruiting
- NCT06367439 — Examining the Effects of Virtual Reality Exercise on Mental Health · NA · completed
- NCT05794789 — "We Are an Active Family": Promoting Child Physical Activity Through Social Identity Formation in the Family System · NA · recruiting
- NCT05738122 — Evaluating the Efficacy of a 60-day Emotion Regulation Journal · NA · completed
- NCT05738109 — Evaluating the Efficacy of a 91-day Self-talk Mental Health Self-care Journal · NA · completed
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 NCT07446231 (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 University of Victoria
- Last refreshed: 3 March 2026
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/NCT07446231.
Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing