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6-week-exercise programme for anterior pelvic tilt in healthy male adults with different anterior pelvic tilt: a controlled trial.

6-week-exercise programme for anterior pelvic tilt in healthy male adults: a controlled trial.

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12618001768280
Acronym
6week-TE-APT
Enrollment
35
Registered
2018-10-26
Start date
2018-11-05
Completion date
2018-11-07
Last updated
2023-07-10

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

Conditions

None listed

Brief summary

This study will test the effectiveness of an intervention to decrease anterior pelvic tilt Arm1: voluntary participants who decide to take part in a 6 week intervention programe which combines manual therapy and active exercises to decrease anterior pelvic tilt.  Arm2: voluntary in-active group that continue with their habitual activities of daily living during the intervention period. After the baseline test both groups will be advise to preserve their regular routines during the 6-week therapeutic intervention. We hypothesized the intervention group will decrease anterior pelvic tilt more than the control group. The decreased anterior pelvic tilt in the intervention group will be proportional to the tilt magnitude, higher for those with higher anterior pelvic tilt and lower or nil for a lowered anterior pelvic tilt.

Interventions

The intervention group participants will be enrolled in a therapeutic programe that has been designed for the purpose of this study. It combines a repertory of standardized exercises that have been previpusly described in scientific literature. This programe of exercises will be conducted in a Hospital and delivered by a physiotherapist who supervise and control each therapeutic session during the intervention period. Each participant will receive 45min therapy per session, in 18 separated sess

The intervention group participants will be enrolled in a therapeutic programe that has been designed for the purpose of this study. It combines a repertory of standardized exercises that have been previpusly described in scientific literature. This programe of exercises will be conducted in a Hospital and delivered by a physiotherapist who supervise and control each therapeutic session during the intervention period. Each participant will receive 45min therapy per session, in 18 separated sessions (three sessions per week, for 6 weeks). The programe involve 2 stages The first from week 1 to three and the second from the fourth to sixth week. The sessions are individual (not in group) and based on 1) active therapeutic exercise (80% of the intervention time) and 2) manual therapy (20% of intervention time). During the first stage all participants will perform 18 therapeutic active exercises and 5 manual therapy passive exercises. During the second stage 19 therapeutic active exercises and 5 manual therapy passive exercises. Exercise progression from the first to the second stage will involve exercise-difficulty-demand and incresed number of repetitions (bouts per exercise). The therapeutic exercises includes: a) active lumbopelvic mobility, b) global hip muscle flexibility, c) hip muscle-strengthening exercises and d) lumbopelvic sensorimotor control exercises. Four flexibility-based-exercises will be developed during the first stage and 4 bouts and 15s position position maintenance, will be perform. In the second stage one flexibility exercise 4 bouts and 15s position maintenance will be perform. Mobility exercises during the first stage are 3 and 2-4 buts and 8 to 12 repetitions per bout will be perform; in the second stage 5 exercises and 2 to 3 bouts and 6, 8 or 12 repetitions will be performed. Both mobility flexibility exercises will be performed to self-perceived mid discomfor, no pain. Strengthening exercises for hip flexors include 5 exercises in the first stage and 4 in the second stage; the number of bouts are 2-3 during the first stage and 3 in the second stage and repetitions per bout will ranged from 6-8 during the first stage to 5-6 during the second stage. Exercises intensity-progression will be adjusted based on percent body weight bearing and/or the use of elastic bands. Posterior pelvic tilt drills will be included only during the second stage with three exercises that will be repeated from 2 two 5 times. The manual therapy includes: soft tissue massage and central lumbar vertebral posterior-anterior mobilization. Soft tissue massage includes 3 exercises both during the first stage and second stage each one of them will be performed two bouts for 30s. Lumbopelvic mobilization include lumbar soft tissue massage and lumbar z-joint mobilization During the intervention period all the participants will be encourage to continue with their habitual routines and regular activities including physical exercise. Adherence to the therapeutic programe will be control by session attendance registry.

Sponsors

Jurdan Mendiguchia Sorabilla
Lead SponsorIndividual

Study design

Allocation
Non-randomised trial
Intervention model
Parallel
Primary purpose
Educational / counselling / training
Masking
Open (masking not used)

Eligibility

Sex/Gender
Male
Age
18 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

Male young, with no mobility limitation. Participants will have anterior pelvic tilt (APT). As it is normal for healthy individuals to possess APT, the average angle of anterior pelvic tilt ranges will vary between them as well.

Exclusion criteria

Low-back pain, have had recent back surgery, and/or are in the midst of an acute low-back flare-up. Participants with strength or mobility deficiencies, where the individual cannot even lift the torso from a forward flexed position to a neutral position. Participants with a high body mass, in which case it would be difficult for the Physiotherapist or Exercise Physiologist, to support the client's suspended upper-body weight. Any neuromusculosqueletical issue at the hip or lower limb that represent a health risk for the participant.

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026