Skip to content

Mindfulness Practice vs Strength Training on Pain, Kinesiophobia and Function Among Sprinters

Effects of Mindfulness Practice With Strength Training on Pain, Kinesiophobia and Function Among Sprinters With Patellofemoral Syndrome

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06240962
Enrollment
30
Registered
2024-02-05
Start date
2023-10-20
Completion date
2024-02-20
Last updated
2024-02-05

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

Conditions

Kinesiophobia, Patellofemoral Pain Syndrome, Resistance Training, Sprinters

Keywords

Mindfulness Practice, Resistance Training, Pain, Sprinters, Patellofemoral Pain Syndrome

Brief summary

The study is randomized and single-blinded. Ethical approval is taken from ethical committee of Riphah International University, Lahore. Participants who meet the inclusion criteria will be enrolled and allocated in group A & B through sealed envelope method by Non-probability Convenient random sampling technique. Subjects in Group A will receive the strength training only. Group B will receive the mindfulness-exercise in addition to the strength training protocol.

Detailed description

The objective of the study is to determine the effects of mindfulness practice with strength training on pain, kinesiophobia and function among sprinters with patellofemoral syndrome. The study is randomized and single-blinded. Ethical approval is taken from ethical committee of Riphah International University, Lahore. Participants who meet the inclusion criteria will be enrolled and allocated in group A & B through sealed envelope method by Non-probability Convenient random sampling technique. Subjects in Group A will receive the strength training only. Group B will receive the mindfulness-exercise in addition to the strength training protocol. Usual pain, pain during stepping, and pain during running will be assessed using visual analog scales. Functional limitations of the knee will be assessed using the Knee Outcome Survey. Fear of movement, pain catastrophizing, and coping strategies will be measured via the Tampa Scale for Kinesiophobia, the Pain Catastrophizing Scale, and the Coping Strategies Questionnaire, respectively. For strength training we will use Muscle-strengthening Exercise Questionnaire Short Form (MSEQ). These outcomes will be assessed at baseline and after 6 weeks The data will be analyzed by SPSS, version 25. Statistical significance is P=0.05.

Interventions

OTHERStrength Training

They will receive the strength training only (6 weeks, 3 sessions/week) that feature training modifications to help control injury-related symptoms.

OTHERMindfulness Exercise

They will receive mindfulness-exercise for 6-week mindfulness intervention in addition to the strength training protocol.

Sponsors

Riphah International University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
SINGLE (Outcomes Assessor)

Masking description

the assessor who will take the readings is blind

Intervention model description

randomized clinical trail

Eligibility

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

Inclusion criteria

* Males and Female between the ages of 18 and 40 years, Report running ≥2 times per week for \>45 minutes or a minimum weekly running distance of 10 km, Present a history of insidious onset of signs and symptoms of PFP in 1 or both knees that was unrelated to trauma for at least 3 months before assessment, score \<85/100 on the Activities of Daily Living Scale and Sports related of the Knee Outcome Survey (KOS-ADLS)

Exclusion criteria

* Intra-articular condition, Coexisting lower limb injury, History of patellar dislocation or knee surgery, Osgood-Schlatter or Sinding- Larsen-Johansson syndrome

Design outcomes

Primary

MeasureTime frameDescription
Knee Painpre and 6 weeks post interventionalUsual pain, pain during stepping and running will be assessed using visual analog scales.
Kinesiophobiapre and 6 weeks post interventionalTampa Scale will be used to assess kinesiophobia.
Physical Functionpre and 6 weeks post interventionalFunctional limitations of the knee will be assessed using the Knee Outcome Survey.

Countries

Pakistan

Contacts

Primary ContactMalia Younas, MS DPT
maliayounas62@gmail.com0325-8292286

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026