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Enrolling By InvitationNCT06977919

NASM OPT for Pectoral Enhancement and Breast Firmness in Non-Athletic Women: An RCT

Efficacy of a 12-Week NASM Optimum Performance Training Program on Pectoral Muscle Strength, Breast Aesthetics, and Low Back Pain in Non-Athletic Women: A Randomized Controlled Trial

Status
Enrolling By Invitation
Phase
N/A
Study type
Interventional
Enrollment
120 (estimated)
Sponsor
University of Sistan and Baluchestan · Academic / Other
Sex
Female
Age
20 Years – 45 Years
Healthy volunteers
Accepted

Summary

This RCT investigates a 12-week NASM OPT program targeting pectoral muscle strength, breast aesthetics (firmness, lift, chest circumference), and low back pain in 120 non-athletic women. The intervention group performed structured resistance training, while the control group engaged in general exercise. Outcomes included pectoral strength (dynamometer), aesthetic satisfaction (Likert scale), and functional performance (push-up test).

Detailed description

Participants were randomized to NASM OPT (3 weekly sessions: stabilization, strength, and hypertrophy phases) or general exercise (brisk walking/aerobics). Measurements at baseline and 12 weeks included pectoral strength, chest circumference, low back pain (VAS), and perceived breast aesthetics.

Conditions

Interventions

TypeNameDescription
BEHAVIORALNASM OPT ProgramThree 60-minute weekly sessions for 12 weeks, progressing through stabilization (weeks 1-4), strength endurance (weeks 5-8), and hypertrophy (weeks 9-12) phases. Exercises included bench presses, chest flyes, and push-ups.
BEHAVIORALGeneral ExerciseThree 60-minute weekly sessions of brisk walking and light aerobics without targeted resistance training.

Timeline

Start date
2025-05-01
Primary completion
2025-08-15
Completion
2025-09-30
First posted
2025-05-18
Last updated
2025-05-18

Locations

1 site across 1 country: Iran

Source: ClinicalTrials.gov record NCT06977919. Inclusion in this directory is not an endorsement.

NASM OPT for Pectoral Enhancement and Breast Firmness in Non-Athletic Women: An RCT (NCT06977919) · Clinical Trials Directory