Skip to content

A study to see whether exercises matched to students personality can improve fitness, regular exercise habits, quality of life and stress recovery among healthcare students from South India

Effect of personality- tailored exercise program on fitness, adherence, quality of life and psychophysiological well-being in South Indian healthcare students- A randomised control trial - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/01/101613
Enrollment
100
Registered
2026-01-20
Start date
Unknown
Completion date
Unknown
Last updated
2026-02-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Intervention1: Personality-matched exercise program: Participants will receive an individualized exercise program based on dominant personality traits assessed using the Big Five Inventory (BFI-44). E

Sponsors

ACS Medical College and Hospital
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Apparently healthy healthcare students aged 18 24 years from a south indian medical college Willing to participate in exercise sessions and assessments Ownership of smartphone for follow-up and adherence monitoring Willingness to provide written informed consent Ability to participate in the study for the full 3 weeks duration

Exclusion criteria

Exclusion criteria: History of diagnosed psychiatric illness or current use of psychiatric medications. Presence of any acute illness or injury at the time of recruitment. Known chronic medical conditions including hypertension, diabetes mellitus, asthma, thyroid disorders, or cardiovascular disease. History of musculoskeletal injury or physical limitation that may interfere with participation in structured exercise. Current participation in structured or supervised exercise programs more than three times per week. Known hypersensitivity to cold exposure or peripheral vascular disorders that may interfere with the Cold Pressor Test (e.g., Raynaud s phenomenon). Use of medications known to affect cardiovascular or stress responses, such as beta-blockers or systemic corticosteroids.

Design outcomes

Primary

MeasureTime frame
Change in stress recovery and cardiorespiratory fitness following the exercise interventionTimepoint: Baseline (pre-intervention) and at the end of 3 weeks (post-intervention)

Secondary

MeasureTime frame
Change in quality of life and psychological well-being following the exercise intervention.Timepoint: Baseline (pre-intervention) and at the end of 3 weeks (post-intervention).;Exercise adherence to the prescribed exercise programTimepoint: Throughout the 3-week intervention period

Countries

India

Contacts

Public ContactDr A Suba

ACS Medical College and Hospital

subagopal.physiology@acsmch.ac.in9487527299

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 7, 2026