NCT07155655

Brief Summary

This pilot randomized controlled trial investigated the influence of motivation combined with motor imagery (MI) or action observation (AO) on lumbo-pelvic strength in asymptomatic adults. The purpose was to explore whether adding a motivational protocol to mental practice strategies could enhance strength outcomes. Forty healthy participants were randomly assigned to one of four groups: motor imagery (MI), action observation (AO), motor imagery with motivation (MIm), or action observation with motivation (AOm). Lumbo-pelvic strength was measured using a dynamometer, while imagery ability was evaluated with the revised Movement Imagery Questionnaire (MIQ-R). Assessments were performed at baseline and post-intervention, with strength additionally measured pre-, intra-, and post-intervention. The trial was conducted between September 2022 and June 2023 at Centro de Estudios Universitarios La Salle, Madrid, Spain, during the investigator's student affiliation. This study is being registered retrospectively to meet ethical and publication requirements.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
40

participants targeted

Target at P50-P75 for not_applicable healthy-volunteers

Timeline
Completed

Started Sep 2022

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

September 18, 2022

Completed
8 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 25, 2023

Completed
9 days until next milestone

Study Completion

Last participant's last visit for all outcomes

June 3, 2023

Completed
2.2 years until next milestone

First Submitted

Initial submission to the registry

August 19, 2025

Completed
16 days until next milestone

First Posted

Study publicly available on registry

September 4, 2025

Completed
Last Updated

September 4, 2025

Status Verified

August 1, 2025

Enrollment Period

8 months

First QC Date

August 19, 2025

Last Update Submit

September 1, 2025

Conditions

Keywords

Motor imagery; Action observation; Motivation; Lumbo-pelvic strength; Pilot trial.

Outcome Measures

Primary Outcomes (1)

  • Lumbo-pelvic strength

    Maximal voluntary contraction of lumbo-pelvic muscles assessed using a dynamometer. Strength was recorded at three time points: baseline, mid-intervention (fourth teletraining session, Week 2), and post-intervention (Week 4, end of program).

    Baseline (Day 1), Mid-intervention (Week 2), and Post-intervention (Week 4, end of program)

Secondary Outcomes (4)

  • Fear of Movement

    Baseline and post-intervention (4 weeks)

  • Physical activity

    Baseline and post-intervention (4 weeks)

  • Self-Efficacy for Physical Activity

    Baseline and post-intervention (4 weeks)

  • Motor Imagery Ability - Visual and Kinaesthetic

    Baseline and post-intervention (4 weeks)

Study Arms (4)

Motor Imagery (MI)

EXPERIMENTAL

Ten asymptomatic participants assigned to a motor imagery training protocol, performed twice weekly for four weeks.

Behavioral: Motor Imagery (MI)

Action Observation (AO)

EXPERIMENTAL

Ten asymptomatic participants assigned to an action observation training protocol, performed twice weekly for four weeks.

Behavioral: Action Observation (AO)

Motor Imagery With Motivation (MIm)

EXPERIMENTAL

Ten asymptomatic participants assigned to motor imagery training combined with a motivational protocol, performed twice weekly for four weeks.

Behavioral: Motor Imagery with Motivation (MIm)

Action Observation With Motivation (AOm)

EXPERIMENTAL

Ten asymptomatic participants assigned to action observation training combined with a motivational protocol, performed twice weekly for four weeks.

Behavioral: Action Observation with Motivation (AOm)

Interventions

Participants followed an audio-guided motor imagery protocol describing the lumbopelvic dynamometer movement. The audio was played three times per session, with pauses for visualization. Training was delivered online via Microsoft Teams, twice weekly for four weeks, in a quiet and focused environment.

Also known as: Mental imagery
Motor Imagery (MI)

Participants viewed three videos of the lumbopelvic dynamometer movement (two third-person, one first-person perspective). Each video was watched three times per session. Training was delivered online via Microsoft Teams, twice weekly for four weeks, with participants instructed to remain silent and focused.

Also known as: Observation training
Action Observation (AO)

Participants followed the MI protocol, combined with a motivational strategy. Intrinsic motivation was provided through self-talk statements, and extrinsic motivation through an audio simulating a weightlifting competition. Each motivational audio was played three times per session. Training was delivered online via Microsoft Teams, twice weekly for four weeks.

Motor Imagery With Motivation (MIm)

Participants followed the AO protocol, combined with the same motivational strategy described for the MIm group (self-talk + extrinsic audio simulation). Each motivational audio was played three times per session. Training was delivered online via Microsoft Teams, twice weekly for four weeks.

Action Observation With Motivation (AOm)

Eligibility Criteria

Age18 Years - 65 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Asymptomatic male and female participants
  • Aged between 18 and 65 years
  • No musculoskeletal, systemic, neurological, cognitive, or psychological disorders affecting the lumbopelvic area

You may not qualify if:

  • Students enrolled in bioscience-related degrees beyond their first year
  • History of pathology or surgery involving the lower limb or lumbar spine
  • Lumbopelvic or lower limb pain within the past three months
  • Illiteracy
  • Pregnant women or those who suspected pregnancy

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Centro Universitario La Salle - Madrid

Madrid, Madrid, 28023, Spain

Location

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Purpose
TREATMENT
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Independent Researcher Sponsor-Investigator

Study Record Dates

First Submitted

August 19, 2025

First Posted

September 4, 2025

Study Start

September 18, 2022

Primary Completion

May 25, 2023

Study Completion

June 3, 2023

Last Updated

September 4, 2025

Record last verified: 2025-08

Locations