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Patellofemoral PainNCT06846125

Mindfulness Training Along Strength Training Among Sprinters With Patellofemoral Pain

A study testing GROUP A: Combined Mindfulness and Strength Training and GROUP B: Strength Training Only in people with Patellofemoral Pain, run by Riphah International University at 1 site in Pakistan.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The study is to find out of the comparative Sprinting-induced patellofemoral pain syndrome (PFPS) causes physical and psychologicalal distress in athletes. While strength training has been used for physical rehabilitation, mindfulness training is a recent addition to rehabilitation science with the potential to… Read more about this study

Who is it for?
Ages 18 to 25 years, women onlyHealthy volunteers can take part
Conditions the study is for
Patellofemoral Pain
What is being tested?
GROUP A: Combined Mindfulness and Strength Training and GROUP B: Strength Training Only
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
34 participants
Where
1 sitePakistan
Study dates
24 Apr 2024to 25 Dec 2024
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 25 years
  • Women only
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Age group between 18 to 25 years.
  • Female runners.
  • PFP conformation check (Single leg squat, and Eccentric step) (24)

Who cannot join

  • Post-surgical condition from the past 6 months
  • Chronic medical condition (cancer, COPD)
  • Players addicted to any drugs or alcohol

Trial locations and contacts

1 site in 1 country.

Pakistan1 site
  • University of Lahore sports complex

    Lahore, Punjab Province, 54000

Other trials in Pakistan

About this study

Official title: Effect of Mindfulness Training Along With Strength Training on Psychological Rehabilitation and Knee Function Among Sprinters With Patellofemoral Pain

The study is to find out of the comparative Sprinting-induced patellofemoral pain syndrome (PFPS) causes physical and psychologicalal distress in athletes. While strength training has been used for physical rehabilitation, mindfulness training is a recent addition to rehabilitation science with the potential to improve both physical AND psychological protocols.

Read the detailed description

Research on the effects of mindfulness and strength training on knee function in sprinters with patellofemoral pain is lacking, despite a wealth of studies on the psychological rehabilitation of athletes. The study's findings indicated that stress reduction and pain management enhance knee function. To improve the physical and psychological elements of sprinters with patellofemoral discomfort, this research assists them integrate mindfulness training with strength training. Strength training to improve knee stability and muscle balance, as well as mindfulness to lessen the psychological effects of pain and stress, can help sprinters with both the mental and physical aspects of patellofemoral pain. Research was being done on this combined approach in this specific population.

Being tested
GROUP A: Combined Mindfulness and Strength Training, GROUP B: Strength Training Only
Keywords
PFPs, Agility strength training, Strength training mindfulness training
Medical subject headings
Patellofemoral Pain Syndrome

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • GROUP A: Combined Mindfulness and Strength TrainingOther

    Week Exercises Reps x Sets 1-2 Mindfulness Training: Breathing exercises, body scans, and meditation. Strength Training: Bodyweight squats, glute bridges, calf raises. 10 x 2 3-4 Mindfulness Training: Guided visualization and mindfulness integration during exercises.

    Strength Training: Weighted squats, hamstring curls, lunges. 12 x 3 5-6 Mindfulness Training: Focus on movement awareness and posture during high-intensity drills.

    Strength Training: Single-leg squats, step-ups, resistance band lateral walks. 15 x 3 7-8 Mindfulness Training: Integration during advanced functional movements. Strength Training: Plyometric box jumps, Bulgarian split squats, deadlifts. 12 x 4

  • GROUP B: Strength Training OnlyOther

    Week Exercises Reps x Sets 1-2 Bodyweight squats, glute bridges, calf raises. 10 x 2 3-4 Weighted squats, hamstring curls, lunges. 12 x 3 5-6 Single-leg squats, step-ups, resistance band lateral walks. 15 x 3 7-8 Plyometric box jumps, Bulgarian split squats, deadlifts. 12 x 4

Study groups in NCT06846125
Study groupRoleWhat they receive
Group AExperimentalNot described
Receives: Other: GROUP A: Combined Mindfulness and Strength Training
Group BPlacebo comparatorNot described
Receives: Other: GROUP B: Strength Training Only

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Numeric Pain Rating Scale

    The 11-point numeric scale ranges from '0' representing one pain extreme (e.g. "no pain") to '10' representing the other pain extreme

    Measured: Baseline, Week 4, and Week 8 (Post-Intervention Assessment)

  2. Knee Range of Motion

    All the Ranges for Knee joint will be measured through Goniometer.

    Measured: Baseline, Week 4, and Week 8 (Post-Intervention Assessment)

  3. Knee Outcome Survey - Sports Activities Scale

    Functional Performance: Evaluated using the Knee Outcome Survey - Sports Activities Scale (SAS)

    Measured: Baseline, Week 4, and Week 8 (Post-Intervention Assessment)

Secondary outcomes (2)
  1. Single-Leg Wall Sit Test

    Functional Endurance: Assessed using the Single-Leg Wall Sit Test (SLWST)

    Measured: Baseline, Week 4, and Week 8 (Post-Intervention Assessment)

  2. Self-Rating Anxiety Scale

    Psychological Well-being: Measured using the Self-Rating Anxiety Scale (SAS)

    Measured: Baseline, Week 4, and Week 8 (Post-Intervention Assessment)

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted25 Feb 2025
  2. Study start24 Apr 2024
  3. Primary completion15 Nov 2024
  4. Study completion25 Dec 2024

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
34 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06846125
Sponsor's protocol ID
REC/RCR&AHS/24/79018
Status last verified
Feb 2025
First submitted
20 Feb 2025
Last updated
25 Feb 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing GROUP A: Combined Mindfulness and Strength Training and GROUP B: Strength Training Only in people with Patellofemoral Pain, run by Riphah International University at 1 site in Pakistan.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 25 Feb 2025. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Pakistan. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Numeric Pain Rating Scale (time frame: Baseline, Week 4, and Week 8 (Post-Intervention Assessment)). The study lists 3 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 25 Feb 2025.

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