NCT07305389

Brief Summary

Affective phenomena, such as core affect, remembered pleasure, or forecasted pleasure, play a key role in promoting physical activity (PA) behaviour, especially among inpatients. The use of music has been shown to be a particularly cost-effective and low-friction approach to promoting positive affective valence during PA. However, interventions using music to improve exercise-related affective phenomena among inpatients are lacking. This study will aim to investigate an intervention that combines the effects of music with the "peak-end rule" on core affective responses (valence and arousal), remembered pleasure, and forecasted pleasure associated with exercise sessions among cardiac rehabilitation inpatients. The primary objective of the present study will be to examine the effect of differentiated music exposure on core affective responses, ratings of perceived exertion and psychophysiological responses to moderate-intensity continuous training (MICT), as well as on associated remembered pleasure, exercise enjoyment, and forecasted pleasure. A secondary objective will be to assess the potential mediating effect of affective valence at the end of the MICT on remembered pleasure and exercise enjoyment. A third objective will be to assess the effect of MICT with or without music on an emotional rating task, together with pupillometric measures. Finally, the study will examine the influence of remembered pleasure on subsequent forecasted pleasure.

Trial Health

77
On Track

Trial Health Score

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

Enrollment
72

participants targeted

Target at P50-P75 for not_applicable

Timeline
9mo left

Started Sep 2024

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

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 Progress70%
Sep 2024Jan 2027

Study Start

First participant enrolled

September 1, 2024

Completed
1.3 years until next milestone

First Submitted

Initial submission to the registry

December 12, 2025

Completed
14 days until next milestone

First Posted

Study publicly available on registry

December 26, 2025

Completed
1.1 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 30, 2027

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

January 30, 2027

Last Updated

December 26, 2025

Status Verified

December 1, 2025

Enrollment Period

2.4 years

First QC Date

December 12, 2025

Last Update Submit

December 12, 2025

Conditions

Keywords

cardiac rehabilitationmusicphysical activityaffective valence

Outcome Measures

Primary Outcomes (1)

  • Affective valence during the moderate intensity continuous training

    Mesured with filling scale (FS)

    22 minutes

Secondary Outcomes (2)

  • Affective arousal during the moderate-intensity continuous training

    25 minutes

  • Rating of perceived exertion during the moderate-intensity continuous training

    5 minutes after each training session

Study Arms (4)

MFH

EXPERIMENTAL

Music in the First Half of the Exercise Session

Other: Music listening during physical exercise

MSH

EXPERIMENTAL

Music in the Second Half of the Exercise Session

Other: Music listening during physical exercise

MT

EXPERIMENTAL

Music Throughout the Exercise Session

Other: Music listening during physical exercise

Control

NO INTERVENTION

Exercice Session without any music

Interventions

Exposure to music played at different phases of the physical activity

MFHMSHMT

Eligibility Criteria

Age50 Years - 75 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • Individuals enrolled in an inpatient 3-week cardiac exercise-based rehabilitation programme
  • Age range 50-75 years
  • Can withstand the study protocol without undue risk
  • Able to provide written consent

You may not qualify if:

  • Contraindication to physical activity in view of the health status
  • Presence of cognitive or psychological disorder
  • Hearing impairment with or without hearing aids

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Hopitaux Universitaires de Genève

Geneva, 1205, Switzerland

RECRUITING

MeSH Terms

Conditions

Motor Activity

Condition Hierarchy (Ancestors)

Behavior

Central Study Contacts

Elena Tessitore, MD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
SUPPORTIVE CARE
Intervention Model
CROSSOVER
Model Details: Randomised controlled trial with repeated-measures and crossover design with full counterbalancing
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
MD

Study Record Dates

First Submitted

December 12, 2025

First Posted

December 26, 2025

Study Start

September 1, 2024

Primary Completion (Estimated)

January 30, 2027

Study Completion (Estimated)

January 30, 2027

Last Updated

December 26, 2025

Record last verified: 2025-12

Locations